| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abdominal fat aspirative biopsy — diagnostic value in familial amyloidotic polyneuropathy, Portuguese type
|
Carvalho, F.
|
|
1996
|
6 |
S1 |
p. S55-
1 p.
|
artikel
|
| 2 |
Abnormal proteolysis in FAF is restricted to the secretory form of gelsolin
|
Kangas, Hannele
|
|
1996
|
6 |
S1 |
p. S34-
1 p.
|
artikel
|
| 3 |
Absence of amyloid from transplanted liver in Met-30 TTR FAP: Evidence from post-mortem specimens
|
Salvi, F.
|
|
1996
|
6 |
S1 |
p. S85-
1 p.
|
artikel
|
| 4 |
A compound heterozygous patient for two TTR mutations, affected with isolated restrictive amyloidotic cardiomyopathy
|
Fertini, A.
|
|
1996
|
6 |
S1 |
p. S23-
1 p.
|
artikel
|
| 5 |
A highly conservative Ile-20 substitution at the dimer-dimer interface selectively reduces stability of the tetrameric transthyretin complex and is associated with familial cardiomyopathy
|
Jenne, Dieter E.
|
|
1996
|
6 |
S1 |
p. S17-
1 p.
|
artikel
|
| 6 |
Altered thyroxine binding to amyloidogenic and non-amyloidogenic transthyretin variants: TTR Met 119 and TTR Pro 55
|
Almeida, Maria Rosário
|
|
1996
|
6 |
S1 |
p. S13-
1 p.
|
artikel
|
| 7 |
A monoclonal antibody recognizing amyloidogenic mutants of transthyretin
|
Goldsteins, Gundars
|
|
1996
|
6 |
S1 |
p. S14-
1 p.
|
artikel
|
| 8 |
A mouse model of familial amyloidotic polyneuropathy type i homozygous for the mutant transthyretin gene
|
Yokoil, K.
|
|
1996
|
6 |
S1 |
p. S32-
1 p.
|
artikel
|
| 9 |
Amyloid polyneuropathy with the TTR Met 30 mutation in an Indonesian family
|
Grateau, G.
|
|
1996
|
6 |
S1 |
p. S37-
1 p.
|
artikel
|
| 10 |
Anaesthetic management of the patient with familial amyloidotic polyneuropathy — experience of 26 liver transplantations
|
Viana, J.S.
|
|
1996
|
6 |
S1 |
p. S72-
1 p.
|
artikel
|
| 11 |
A new and sensitive tool for autonomic dysfuntion: analysis by radiolabelled meta-iodobenzylguanidine (MIBG) in patients with familial amyloidotic polyneuropathy (FAP) type i
|
Obayashi, Kounen
|
|
1996
|
6 |
S1 |
p. S66-
1 p.
|
artikel
|
| 12 |
A new transthyretin (TTR) variant-TTR cysteine 104
|
Torres, M.F.
|
|
1996
|
6 |
S1 |
p. S21-
1 p.
|
artikel
|
| 13 |
Anticipation and multiple origins in familial amyloid polyneuropathy with transthyretin-Met30 in Japan
|
Yamamoto, Kanji
|
|
1996
|
6 |
S1 |
p. S42-
1 p.
|
artikel
|
| 14 |
Apolipoprotein all levels in portuguese patients with FAP
|
Saraiva, M.J.
|
|
1996
|
6 |
S1 |
p. S26-
1 p.
|
artikel
|
| 15 |
Apolipoprotein e genotype and familial amyloidotic polyneuropathy type I
|
Satoh, Shun-ichi
|
|
1996
|
6 |
S1 |
p. S27-
1 p.
|
artikel
|
| 16 |
Assessment of autonomic dysfunction in familial amyloidotic polyneuropathy: A challenge
|
Fonseca, C.
|
|
1996
|
6 |
S1 |
p. S48-
1 p.
|
artikel
|
| 17 |
Author index
|
|
|
1996
|
6 |
S1 |
p. S93-S94
2 p.
|
artikel
|
| 18 |
Author index
|
|
|
1996
|
6 |
S1 |
p. S59-S61
3 p.
|
artikel
|
| 19 |
Bindings of mutant transthyretin with high density lipoprotein (HDL) and low density lipoprotein (LDL): a novelfunction of lipoprotein
|
Tanaka, Yoshiya
|
|
1996
|
6 |
S1 |
p. S26-
1 p.
|
artikel
|
| 20 |
Biochemical assessment of transthyretin immunoapheresis for the treatment of FAP
|
Costa, P.M.P.
|
|
1996
|
6 |
S1 |
p. S56-
1 p.
|
artikel
|
| 21 |
Can variance-EKG predict circulatory complications during liver transplantation in FAP patients?
|
Eleoborg, Lennart
|
|
1996
|
6 |
S1 |
p. S76-
1 p.
|
artikel
|
| 22 |
Changed affinity of apolipoprotein al to high density lipopotein (HDL) in patients with familial amyloidotic polyneuropathy (FAP) (Met30, Gln89, Pro36, Thr34)
|
Nakamura, Masaaki
|
|
1996
|
6 |
S1 |
p. S25-
1 p.
|
artikel
|
| 23 |
Change in the age of onset in patients with familial amyloidotic polyneuropathy (FAP) type i in Japan
|
Tashima, Kazuhiro
|
|
1996
|
6 |
S1 |
p. S43-
1 p.
|
artikel
|
| 24 |
Changes in variant transthyretin levels in patients with familial amyloidotic polyneuropathy (FAP) type i following liver transplantan
|
Ando, Yukio
|
|
1996
|
6 |
S1 |
p. S85-
1 p.
|
artikel
|
| 25 |
Characterization of the initiating event in the pathogenesis of geisolin-related amyloidosis (FAF) by in vitro expression analysis
|
Paunio, Tiina
|
|
1996
|
6 |
S1 |
p. S33-
1 p.
|
artikel
|
| 26 |
Circulatory instability during liver transplantation; impact of autonomic dysfunction evaluated by spectral analysis of RR-interval. A preliminary report
|
Suhr, Ole
|
|
1996
|
6 |
S1 |
p. S73-
1 p.
|
artikel
|
| 27 |
Clearance of variant transthyretin from serum after liver transplantation in patients with familial amyloidotic polyneuropathy
|
Uemichi, T.
|
|
1996
|
6 |
S1 |
p. S89-
1 p.
|
artikel
|
| 28 |
Clinical and genetic study of familial amyloidotic polyneuropathy with Ile 50 TTR mutation in Japanese family
|
Okamoto, Naoyuki
|
|
1996
|
6 |
S1 |
p. S36-
1 p.
|
artikel
|
| 29 |
Clinical and morphological findings in the aqueous outflow system and cornea in familial amyloidotic polyneuropathy
|
Tavares, M.A.
|
|
1996
|
6 |
S1 |
p. S50-
1 p.
|
artikel
|
| 30 |
Clinical and neurophysiologic evaluation scores in familial amyloidotic polyneuropathy
|
Conceiçã, I.
|
|
1996
|
6 |
S1 |
p. S66-
1 p.
|
artikel
|
| 31 |
Clinical course and outcome in patients with familial amyoid polyneuropathy (FAP) TTR Met 30 on regular dialysis
|
Beirão, I.
|
|
1996
|
6 |
S1 |
p. S53-
1 p.
|
artikel
|
| 32 |
Coexistence of type i familial amyloid polyneuropathy and spinocerebellar ataxia type i. Pathological study and gene analysis of a Japanese family
|
Ikeda, Shu-ichi
|
|
1996
|
6 |
S1 |
p. S40-
1 p.
|
artikel
|
| 33 |
Comparative catabolism and stability of TTR Met30 and TTR Met119
|
Alves, I.L.
|
|
1996
|
6 |
S1 |
p. S19-
1 p.
|
artikel
|
| 34 |
Compound heterozygotes of transthyretin Met30 and transthyretin Met119 are protected from the devastating effects of familial amyloid polyneuropathy
|
Coelho, Teresa
|
|
1996
|
6 |
S1 |
p. S20-
1 p.
|
artikel
|
| 35 |
Compound heterozygoty in patients with TTR-related amyloidosis
|
Alves, I.L.
|
|
1996
|
6 |
S1 |
p. S19-
1 p.
|
artikel
|
| 36 |
Corino-andrade disease (familial amyloidotic polineuropathy type i) in Spain. Urological and andrological disorders. Clinics and urodinamics findings. Treatment with hepatic transplantation
|
Hita Villaplana, G.
|
|
1996
|
6 |
S1 |
p. S81-
1 p.
|
artikel
|
| 37 |
Correlation between autonomic abnormalities in familial amyloidotic polineuropathy (FAP) — Portuguese type
|
Alves, M.
|
|
1996
|
6 |
S1 |
p. S47-
1 p.
|
artikel
|
| 38 |
Demonstration of mutant TTR(Ala47) in spinal fluid and its absence in plasma after liver transplantation
|
Altland, K.
|
|
1996
|
6 |
S1 |
p. S86-
1 p.
|
artikel
|
| 39 |
Detection of reverse flow by duplex ultrasonography in orthostatic hypotenssion in familial amyloidotic polyneuropathy (FAP) type i
|
Yonehara, Toshiro
|
|
1996
|
6 |
S1 |
p. S54-
1 p.
|
artikel
|
| 40 |
Development of lines of transgenic mice expressing the human transthyretin Ser84 variant
|
Waits, R.P.
|
|
1996
|
6 |
S1 |
p. S31-
1 p.
|
artikel
|
| 41 |
Diagnostic value of skin and nerve biopsy in familial amyloid polyneuropathy
|
Coelho, Teresa
|
|
1996
|
6 |
S1 |
p. S55-
1 p.
|
artikel
|
| 42 |
Dissociation and denaturation of transthyretin
|
Goldsteins, Gundars
|
|
1996
|
6 |
S1 |
p. S15-
1 p.
|
artikel
|
| 43 |
Distribution of transthyretin in the blood of vertebrates
|
Richardson, Samantha J.
|
|
1996
|
6 |
S1 |
p. S11-
1 p.
|
artikel
|
| 44 |
Do patients (pts) with familial amyloid polyneuropathy (FAP) treated with orthotopic liver transplant (OLTx) have less rejection than transplanted patients for liver diseases?
|
Freire, A.
|
|
1996
|
6 |
S1 |
p. S87-
1 p.
|
artikel
|
| 45 |
Editorial Board
|
|
|
1996
|
6 |
S1 |
p. IFC-
1 p.
|
artikel
|
| 46 |
Effect of liver transplantation on autonomic dysfunction in familial myloidotic polyneuropathy type i (Met30)
|
Ando, Yukio
|
|
1996
|
6 |
S1 |
p. S82-
1 p.
|
artikel
|
| 47 |
Efficacy of l-threo-dihydroxyphenylserine in the improvement of orthostatic tolerance in familial amyloidotic polyneuropathy
|
Carvalho, M.J.
|
|
1996
|
6 |
S1 |
p. S57-
1 p.
|
artikel
|
| 48 |
Electromyographic endings in Italian families with transthyretin (TTR)-Related familial amyloid polyneuropathy (FAP)
|
Montagna, P.
|
|
1996
|
6 |
S1 |
p. S53-
1 p.
|
artikel
|
| 49 |
Electrophiological chanes in the spinal cord in patients with familial amyloidotic polyneuropathy (FAP) type i
|
Yamashita, Taro
|
|
1996
|
6 |
S1 |
p. S51-
1 p.
|
artikel
|
| 50 |
Endocrine cells in rectal biopsies from patients with familial amyloidotic polyneuropathy
|
El-Salhy, Magdy
|
|
1996
|
6 |
S1 |
p. S46-
1 p.
|
artikel
|
| 51 |
Epidemiological study of familial amyloidotic polyneuropathy (FAP) in Kumamoto focus, Japan
|
Araki, Shukuro
|
|
1996
|
6 |
S1 |
p. S39-
1 p.
|
artikel
|
| 52 |
Epidemiology and genetic analysis in patients with familial amyloid polyneuropathy (FAP) type i and end-stage renal disease: Can we predict kidney involvement?
|
Lobato, L.
|
|
1996
|
6 |
S1 |
p. S51-
1 p.
|
artikel
|
| 53 |
Evaluation of liver transplantation in familial amyloid polyneuropathy
|
Adams, D.
|
|
1996
|
6 |
S1 |
p. S76-
1 p.
|
artikel
|
| 54 |
Factors affecting outcome of liver transplantation in familial amyloidotic polyneuropathy
|
Suhr, Ole
|
|
1996
|
6 |
S1 |
p. S90-
1 p.
|
artikel
|
| 55 |
Familial amyloedotic polyneuropathy-portuguese type: Cardiac involvement of potential candidates to liver transplant
|
Morais, H.
|
|
1996
|
6 |
S1 |
p. S69-
1 p.
|
artikel
|
| 56 |
Familial amyloidotic polineuropathy (FAP) : Renal transplantation in a liver graft patient
|
Ribeiro, Sílvia
|
|
1996
|
6 |
S1 |
p. S81-
1 p.
|
artikel
|
| 57 |
Familial amyloidotic polyneuropathy, Swedish type: variations in amyloid distribution in relation to transthyretin fragmentation
|
Westermark, Per
|
|
1996
|
6 |
S1 |
p. S27-
1 p.
|
artikel
|
| 58 |
Familial amyloid polyneuropathy (FAP) — type i in póvoa do varzim and vila do conde: A disease in expansion
|
Sousa, A.
|
|
1996
|
6 |
S1 |
p. S42-
1 p.
|
artikel
|
| 59 |
FAP i treated by liver transplant (18 cases): Surgical morbidity and mortality
|
Ramirez, P.
|
|
1996
|
6 |
S1 |
p. S89-
1 p.
|
artikel
|
| 60 |
FAP Met 30 in Sweden.-epidemiological, biochemical, clinical and therapeutical studies-a survey
|
Holmgren, Gösta
|
|
1996
|
6 |
S1 |
p. S38-
1 p.
|
artikel
|
| 61 |
Favorable outcome of myocardial amyloid infiltration in FAP compared to al amyloidosis.-a blinded echocardiographic study
|
Dubrey, S.W.
|
|
1996
|
6 |
S1 |
p. S45-
1 p.
|
artikel
|
| 62 |
Five kindreds with variant fibrinogen presenting renal amyloidosis
|
Uemichi, T.
|
|
1996
|
6 |
S1 |
p. S35-
1 p.
|
artikel
|
| 63 |
Four siblings from the same family with FAP i TTR Ala-71 treated by liver transplantation
|
Lopez, Andreu F.
|
|
1996
|
6 |
S1 |
p. S75-
1 p.
|
artikel
|
| 64 |
Further characterization of transgenic mice, carrying the human TTR Met 30 gene under the control of mouse metalothionein promoter gene, lacking amyloid deposition
|
Bonifácio, Maria João
|
|
1996
|
6 |
S1 |
p. S32-
1 p.
|
artikel
|
| 65 |
Genetic models for variation of age at onset in familial amyloid polyneuropathy
|
Sousa, Alda
|
|
1996
|
6 |
S1 |
p. S41-
1 p.
|
artikel
|
| 66 |
Genetics aspects of FAP in France. Five years experience of one laboratory
|
Grateau, G.
|
|
1996
|
6 |
S1 |
p. S37-
1 p.
|
artikel
|
| 67 |
Hemodynamic response to hepatic vascular exclusion during liver transplant in patients with familial amyloidotic polineuropathy
|
Acosta, F.
|
|
1996
|
6 |
S1 |
p. S70-
1 p.
|
artikel
|
| 68 |
Hepatic transplantation in familial amyloidotic polyneuropathy: Assessment of autonomic function
|
Carvalho, M.J.
|
|
1996
|
6 |
S1 |
p. S68-
1 p.
|
artikel
|
| 69 |
H NMR structural studies of cystine-linked peptide fragment 71–93 of transthyretin and effects of a Ser84 substitution implicated in familial amyloidotic polyneuropathy
|
Craik, David J.
|
|
1996
|
6 |
S1 |
p. S9-
1 p.
|
artikel
|
| 70 |
Human plasma transthyretin (TTR) is composed of many different molecular species with modifiable stability
|
Altland, Klaus
|
|
1996
|
6 |
S1 |
p. S15-
1 p.
|
artikel
|
| 71 |
Impact of gastrointestinal dysfunction on survival after liver transplantation in familial amyloidotic polyneuropathy
|
Suhr, Ole
|
|
1996
|
6 |
S1 |
p. S68-
1 p.
|
artikel
|
| 72 |
Impact of liver transplantation on survival in familial amyloidotic polyneuropathy
|
Suhr, Ole
|
|
1996
|
6 |
S1 |
p. S90-
1 p.
|
artikel
|
| 73 |
Impact of transthyretin Met 111 and Ser 6 mutations on the serum levels of thyroxine and transhyretin, determined in a Danish family with inherited amyloid cariomyopathy
|
Nordvåg, Bjørn-Yngvar
|
|
1996
|
6 |
S1 |
p. S13-
1 p.
|
artikel
|
| 74 |
Improvement of familial amyloid neuropathy following liver transplantation
|
Bergethon, P.R.
|
|
1996
|
6 |
S1 |
p. S84-
1 p.
|
artikel
|
| 75 |
Infections complicating liver transplantation (LP) in familial amyloid polyneuropathy (FAP)
|
Morbey, A.
|
|
1996
|
6 |
S1 |
p. S87-
1 p.
|
artikel
|
| 76 |
In frame deletion in the transthyretin gene (ΔV122) associated with amyloidotic polyneuropathy
|
Uemichi, T.
|
|
1996
|
6 |
S1 |
p. S21-
1 p.
|
artikel
|
| 77 |
In vitro amyloid fibre, formation from transthyretin: the influence of ions and the amyloidogenicity of TTR variants
|
Bonifácio, Maria João
|
|
1996
|
6 |
S1 |
p. S29-
1 p.
|
artikel
|
| 78 |
In vivo immunoadsorption of transthyretin in familial amyloidotic polyneuropathy TTR Met 30: Preliminary clinical experience
|
Lobato, L.
|
|
1996
|
6 |
S1 |
p. S56-
1 p.
|
artikel
|
| 79 |
Is an amyloidogenic substrate enough? Transgenic mice producing human TTR Pro 55 do not develop amyloid
|
Teng, Mei-hui
|
|
1996
|
6 |
S1 |
p. S30-
1 p.
|
artikel
|
| 80 |
Is orthotopic liver transplant (OLTx) a good therapy for familial amyloid polineuropathy? Lisbon experience
|
Monteiro, E.
|
|
1996
|
6 |
S1 |
p. S80-
1 p.
|
artikel
|
| 81 |
Is the nucleotide 654 of the geisolin gene a mutational hot spot?
|
Paunio, Tiina
|
|
1996
|
6 |
S1 |
p. S34-
1 p.
|
artikel
|
| 82 |
Is the patient with familial amyloidotic polyneuropathy a high risk patient for awareness and recall of intraoperative events?
|
Viana, J.S.
|
|
1996
|
6 |
S1 |
p. S75-
1 p.
|
artikel
|
| 83 |
Liver transplantation for familial amyloidotic polyneuropathy in Greece
|
Tzagournissakis, M.
|
|
1996
|
6 |
S1 |
p. S84-
1 p.
|
artikel
|
| 84 |
Liver transplantation for familial amyloid polyneuropathy — report from the world registry
|
Ericzon, Bo-Göran
|
|
1996
|
6 |
S1 |
p. S65-
1 p.
|
artikel
|
| 85 |
Liver transplantation for transthyretin amyloidosis: Experience from Indiana university
|
Benson, M.D.
|
|
1996
|
6 |
S1 |
p. S79-
1 p.
|
artikel
|
| 86 |
Liver transplantation for two Japanese patients with familial amyloidotic polyneuropathy with Ile 50 TTR mutation and Met 30 TTR mutation
|
Ikegawa, Shinichi
|
|
1996
|
6 |
S1 |
p. S83-
1 p.
|
artikel
|
| 87 |
Liver transplantation in 13 F.A.P. patients: Surgical technique and complications
|
Andrade, J.R.
|
|
1996
|
6 |
S1 |
p. S72-
1 p.
|
artikel
|
| 88 |
Liver transplantation in FAP type i Brazilian patients
|
Cruz, M.W.
|
|
1996
|
6 |
S1 |
p. S82-
1 p.
|
artikel
|
| 89 |
Liver transplantation in Swedish FAP patients. A follow up study of 33 patients
|
Lars, Wikström
|
|
1996
|
6 |
S1 |
p. S78-
1 p.
|
artikel
|
| 90 |
Liver transplantation of familiar amyloidoitic polineuropaty (FAP), Portuguese type. Clinical results of transplantation; ultrastural findings of FAP patients
|
Campos, M.Celeste Dias
|
|
1996
|
6 |
S1 |
p. S86-
1 p.
|
artikel
|
| 91 |
Living related liver transplantation for adults: Selection of living donor for the patient with hereditary diseases
|
Matsunami, H.
|
|
1996
|
6 |
S1 |
p. S69-
1 p.
|
artikel
|
| 92 |
Living-related liver transplantation for the patients with familial amyloid polyneuropathy
|
Takei, Yo-ichi
|
|
1996
|
6 |
S1 |
p. S80-
1 p.
|
artikel
|
| 93 |
Management of rhythm disturbances in familial amyloidotic polyneuropathy patients in active list of liver transplant
|
Morais, H.
|
|
1996
|
6 |
S1 |
p. S74-
1 p.
|
artikel
|
| 94 |
Molecular genetics of transthyretin-associated senile cardiac amyloidosis in blacks
|
Bauxbaum, J.
|
|
1996
|
6 |
S1 |
p. S22-
1 p.
|
artikel
|
| 95 |
Most cases of familial amyloidotic polyneuropathy (FAP) are associated with amino acid substitutions destabilizing the folded state of transthyretin monomers
|
Altland, K.
|
|
1996
|
6 |
S1 |
p. S17-
1 p.
|
artikel
|
| 96 |
Natural history of heart involvement in Portuguese familial amyloidotic polyneuropathy
|
Fonseca, C.
|
|
1996
|
6 |
S1 |
p. S45-
1 p.
|
artikel
|
| 97 |
Need for pacemaker during anaesthesia in FAP patients?
|
Eleborg, Lennart
|
|
1996
|
6 |
S1 |
p. S71-
1 p.
|
artikel
|
| 98 |
Neuropathic pain a typical early symptom in late onset patients with familiar amyloidotic polyneuropathy
|
Carvalho, Mamede
|
|
1996
|
6 |
S1 |
p. S52-
1 p.
|
artikel
|
| 99 |
Neurophysiological evaluation of sexual dysfunction in familial amyloidotic polyneuropathy (FAP)
|
Alves, M.
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3 New amyloidogenic TTR mutations: Pro12, Glu18, and Val33
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Booth, D.R.
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New clinical scale of patients with familial amyloidotic polyneuropathy (FAP) type i
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Tashima, Kazuhiro
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Norepinephrine levels in patients with familial amyloidotic polyneuropathy (FAP) undergoing liver transplantation (LT)
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Diaz, J.
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Normal and variant transthyretin in a patient with familial amyloidotic polyneuropathy: DNA, mRNA, serum, and amyloid deposits
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Ocular manifestation of familial amyloidotic polyneuropathy (FAP) type i : long term follow up
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Ando, Eiko
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On the mechanism of transthyretin amyloid fibril formation
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Kelly, Jeffery W.
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Patterns of cardiac involvement in type i familial amyloidotic polyneuropathy
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Carvalho, A.
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Plasma β-endorphin levels during orthotopic liver transplantation (OLT) in patients with familial amyloidotic polyneuropaty (FAP)
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Acosta, F.
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Plasma retinol binding protein levels in individuals with transthyretin gene mutations
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Waits, R.P.
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Post translational modification of serum TTR
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Hutchinson, W.L.
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Premortem recognition of systemic senile amyloidosis with cardiac involvement
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Kyle, Robert A.
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Presymptomatic gene testing and genetic counselling of familial amyloid polyneuropathy. A trial on Japanese kindreds
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Hanaoka, Naoko
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Pre-transplant cardiovascular evaluation of patients with familial amiloidotic polyneuropathy portuguese type
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Sá-Nogueira, J.
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Proteins and other components of vitroeous and tissue fibrils in familial amyloidosis type 1(transthyretin, TTR Met30)
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Thylén, Christina
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Pulmonary artery catheterisation in familial amyloidotic polyneuropathy — data of ten patients before liver transplantation
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Viana, J.S.
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Quality of life after liver transplantation in familial amyloidotic polyneuropathy
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Jonsén, Elisabeth
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Recurrent arterial thrombosis on three liver trausplants on a same patient with FAP
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Mira, Paulo S.
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Rejection and infection after liver transplantation (LT) for familial amyloid polyneuropathy (FAP)
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Saliba, F.
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Renal involvement in amyloid polyneuropathy. Implications for pre-liver transplantation evaluation
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Larue, J.R.
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Report on liver transplantation performed in 18 patients with familial amyloidotic polyneuropathy
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Munar-Ques, M.
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Report on 24 patients with liver transplantation for FAP in the United States
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Lewis, W.David
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Results of liver transplantation in familial amyloidotic polyneuropathy (FAP) type i —12 cases
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Sales Luis, M.L.
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Role of autonomic nervous system in circadian blood pressure variation
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Carvalho, M.J.
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Role of nanc nerves in the gastrointestinal function inpatients with familial amyloidotic polyneuropathy (FAP) type i
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Nakamura, Kenji
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Role of nitric oxide in controlling peripheral blood flow of patients wtth familial amyloidotic polyneuropathy (FAP)type i
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Yamashita, Taro
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1996
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SAP Scintigraphy in 43 patients with TTR-associated FAP
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Hawkins, P.N.
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1996
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Scanning of tranthyretin mutations on Alzheimer's samples
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Palha, J.A.
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Second international workshop on liver transplantation in FAP
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Selection criteria for liver transplantation in patients with familial amyloidotic polyneuropathy
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Munar-Qués, M.
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Severe renal failure complicating liver transplantation (LT) in familial amyloidotic polyneuropathy (FAP)
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Ribeiro, S.
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Structural alterations in ile-122 and Pro-55 variant TTRs: their importance in amyloid formation
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Damas, A.M.
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Structure and evolution of transthyretin
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Structure, function and metabolism of transthyretin
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Benson, M.D.
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Tertiary structures of three amyloidogenic transthyretin variants and implications for amyloid fibril formation
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The crystal structure of Met-119 variant transthyretin
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The first structure of an avian transthyretin : Similarities and differences shown by the human and chicken proteins
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Sunde, Margaret
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The heart in familial amyloidotic polyneuropathy portuguese type
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Fonseca, C.
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The molecular structure of the FAP fibril
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Serpell, Louise
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The role of immuno-hemoterapeut in liver transplantation
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Cordeiro, Alice Lopes
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The severity and distribution of amyloid deposition in the late-onset familial amyloidotic polyneuropathy (FAP) — a clinicopathological analysis of three autopsy cases
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Takahashi, Kiyoshi
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Title: Familial amyloid polyneuropathy treated with orthotopic liver transplantation: Neurophysiological improvement
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de Mingo, P.
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Transgenic study for a role of Cys-10 in amyloidosis of Met-30 TTR
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Takaoka, Yutaka
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Transthyretin amyloid fibril formation: effects of coprecipitation with different transthyretin fragmentS
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Gustavsson, Åsa
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Transthyretin and availability of thyroxine to the brain
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Palha, J.A.
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Transthyretin fibrils and synthetic peptide fibrils
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Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy
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Reilly, M.M.
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Transthyretin gene expression and function in choroid plexus
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Schreiber, G.
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Transthyretin Met 30 in a form of late-onset cardiac amyloidosis
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Rose, C.
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Transthyretin ( TTR ) as nutritional indicator
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TTR Ile 20, a new variant associated with cardiac amyloidosis
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Jacobson, Daniel R.
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TTR mutations in 2 patients wtph a clinical diagnosis of senile cardiac amyloidosis
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Persey, M.R.
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Two new mutations in the transthyretin gene, leading to polyneuropathy and cardiomyopathy in two unrelated ITalian families
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Patrosso, M.C.
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Two transthyretin variants in a danish family with inherited amyloid cardiomyopathy
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Nordvåg, Bjørn-Yngvar
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UK experience of liver transplantation in FAP
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Hawkins, P.N.
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Unusual phenotypic variability within the same family: Variable penetrance and variable clinical expression
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Barros, José
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Up-to-date report on the Majorcan focus of familial amyloidotic polyneuropathy
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Munar-Qués, M.
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Use of mouse models to analyse the molecular bases of familial amyloidotic polyneuropathy type I
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Maeda, S.
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UVCD and thermal stability analysis of human serum variant transthyretin (Met 30) compared with normal
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Variability of clinical expression in familial amyloid polyneuropathy
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Coelho, Teresa
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Variable eipressivity in Met-30 Japanese patients with familial amyloidotic polyneuropaty in kumamoto
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Tawara, Satoru
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Visceral orthostatic hypotension in patients with familial amyloidotic polyneuropathy (FAP) type i
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Terazaki, Hisayasu
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1996
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