| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Phase III Extension Study of Aldurazyme®(Laronidase) in Mucopolysaccharidosis I
|
Clarke, L.A.
|
|
2007
|
|
SC |
p. S111-
1 p.
|
artikel
|
| 2 |
Beyond the Primary Biochemical Defect in Type 1 Gaucher Disease
|
Aerts, Johannes M.F.G.
|
|
2007
|
|
SC |
p. S77-S78
2 p.
|
artikel
|
| 3 |
Brain Involvement—The Ultimate Challenge
|
Mengel, Eugen
|
|
2007
|
|
SC |
p. S95-
1 p.
|
artikel
|
| 4 |
Comprehensive Disease Management Model in Heterogeneous Progressive Disease, Exemplified by Gaucher Disease
|
Mistry, Pramod K.
|
|
2007
|
|
SC |
p. S79-S80
2 p.
|
artikel
|
| 5 |
Designing Protein Therapies: Lessons Learned from Cerezyme® for Gaucher Disease
|
Edmunds, Tim
|
|
2007
|
|
SC |
p. S75-S76
2 p.
|
artikel
|
| 6 |
Enzyme Replacement Therapy and Fabry Kidney Disease
|
Warnock, David G.
|
|
2007
|
|
SC |
p. S96-S98
3 p.
|
artikel
|
| 7 |
Enzyme Replacement Therapy in Mucopolysaccharidosis Type I: The Sooner the Better
|
Coppa, Giovanni V.
|
|
2007
|
|
SC |
p. S83-
1 p.
|
artikel
|
| 8 |
Fabry Disease in Pediatrics: The Need for Early Intervention
|
Wijburg, Frits A.
|
|
2007
|
|
SC |
p. S105-S106
2 p.
|
artikel
|
| 9 |
Foreword
|
Bodamer, Olaf
|
|
2007
|
|
SC |
p. S73-
1 p.
|
artikel
|
| 10 |
Hematologic and Hemato-Oncologic Aspects of Gaucher Disease
|
Hughes, Derralynn
|
|
2007
|
|
SC |
p. S88-S90
3 p.
|
artikel
|
| 11 |
Hypertrophic Cardiomyopathy in Anderson-Fabry Disease
|
Cecchi, Franco
|
|
2007
|
|
SC |
p. S93-S94
2 p.
|
artikel
|
| 12 |
Initial Therapy Response of 6 Months of Enzyme Replacement Therapy in 11 Juvenile/Adult M. Pompe Patients
|
Hartung, Ralf
|
|
2007
|
|
SC |
p. S86-S87
2 p.
|
artikel
|
| 13 |
Longer Survival by Enzyme Replacement Therapy Unmasks the Underrecognition of Otoneurologic Involvement in Infantile-Onset Pompe Disease
|
Mandel, Hanna
|
|
2007
|
|
SC |
p. S109-S110
2 p.
|
artikel
|
| 14 |
Lysosomal Storage Disorders—A Vision of the Future
|
Smith, Alan
|
|
2007
|
|
SC |
p. S74-
1 p.
|
artikel
|
| 15 |
Mucopolysaccharidosis I Patient Narratives
|
Lawes, Rachel
|
|
2007
|
|
SC |
p. S99-S100
2 p.
|
artikel
|
| 16 |
Pompe Disease: A Continuum of Clinical Phenotypes
|
Hagemans, Marloes
|
|
2007
|
|
SC |
p. S103-S104
2 p.
|
artikel
|
| 17 |
Successful Pregnancy on Enzyme Replacement Therapy with Cerezyme®
|
Mrsić, Mirando
|
|
2007
|
|
SC |
p. S84-S85
2 p.
|
artikel
|
| 18 |
The Bone in Gaucher Disease
|
Weinreb, Neal J.
|
|
2007
|
|
SC |
p. S91-S92
2 p.
|
artikel
|
| 19 |
The Enhancement of Coping Skills and Compliance to Treatment in Adolescents with a Chronic Serious Disease
|
Last, Bob F.
|
|
2007
|
|
SC |
p. S107-S108
2 p.
|
artikel
|
| 20 |
Treatment Goals at Different Stages of Fabry Disease Progression
|
Wanner, Christoph
|
|
2007
|
|
SC |
p. S81-S82
2 p.
|
artikel
|
| 21 |
Type 1 Nonneuronopathic Gaucher Disease in Children
|
Kaplan, Paige
|
|
2007
|
|
SC |
p. S101-S102
2 p.
|
artikel
|
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