| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aims and Scope
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141 |
S1 |
p.
|
artikel
|
| 2 |
2024 Conference Planning Committee
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|
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|
141 |
S1 |
p.
|
artikel
|
| 3 |
Editorial Board
|
|
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|
141 |
S1 |
p.
|
artikel
|
| 4 |
Front Cover
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|
141 |
S1 |
p.
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artikel
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| 5 |
GMDI, organization and membership
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141 |
S1 |
p.
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artikel
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| 6 |
O.1 A survey: nutrition management of children less than five years of age with glycogen storage disease type I
|
Sowa, M
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141 |
S1 |
p.
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artikel
|
| 7 |
O.3 Dietary intake among patients with long-chain 3-hydoxyacyl-CoA dehydrogenase deficiency (LCHADD)
|
Sim, E
|
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|
141 |
S1 |
p.
|
artikel
|
| 8 |
O.2 Protein requirements in phenylketonuria adults and bioavailability of glycomacropeptide compared to an L-amino acid based product
|
Turki, A
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141 |
S1 |
p.
|
artikel
|
| 9 |
P.24 A case of missed PKU
|
Mofidi, S
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141 |
S1 |
p.
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artikel
|
| 10 |
P.5 Amino acid levels and nutritional outcomes in children with hereditary tyrosinemia type 1
|
Brockett, J
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141 |
S1 |
p.
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artikel
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| 11 |
P.7 A 12-month review of using a tablet protein substitute preparation in the treatment of tyrosinemia
|
Daly, A
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|
141 |
S1 |
p.
|
artikel
|
| 12 |
P.51 Analyzing outcomes of plant-based enteral nutrition with 50:50 MCT ratio in patients with mitochondrial disorders
|
Kozek, A
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141 |
S1 |
p.
|
artikel
|
| 13 |
P.18 A novel autosomal dominantly inherited variant in BCKDK leads to biochemical maple syrup urine disease: case reports of two families
|
Kopesky, JJ
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141 |
S1 |
p.
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artikel
|
| 14 |
P.14 APHENITY extension study dietary phe tolerance assessment design using 3-day diet records: an interim report
|
Hollander, S
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141 |
S1 |
p.
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artikel
|
| 15 |
P.47 Association between cobalamin deficiency detected through newborn screening and creatine levels in mothers and their offspring in the neonatal period
|
Tosi, M
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|
141 |
S1 |
p.
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artikel
|
| 16 |
P.54 Blenderized tube feeding in metabolic patients: survey results from metabolic dietitians in the U.S.
|
Powers, R
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|
141 |
S1 |
p.
|
artikel
|
| 17 |
P.28 Blood phenylalanine control in patients with phenylketonuria in Europe: is it a changing landscape?
|
Pinto, A
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141 |
S1 |
p.
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artikel
|
| 18 |
P.30 Case-based educational model identifies need for nutritional management guidelines of patients with glutaric acidemia type 1 after basal ganglia stroke
|
Ryan, LM
|
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|
141 |
S1 |
p.
|
artikel
|
| 19 |
P.29 Case report: high protein requirements in maternal phenylketonuria
|
Roberts, P
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|
141 |
S1 |
p.
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artikel
|
| 20 |
P.42 Case study of newborn with LCHAD deficiencyand initiation of oral triheptanoin: dietary strategies over the first year of life
|
Curran, A
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|
141 |
S1 |
p.
|
artikel
|
| 21 |
P.36 Clinical experiences in transitioning PKU patients from second to third stage protein substitutes: a global survey
|
Nas, O Yilmaz
|
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|
141 |
S1 |
p.
|
artikel
|
| 22 |
P.11 Comparison of nutritional status and metabolic control in PKU infants with breastmilk vs infant formula in Mexico
|
Guillén-López, S
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|
141 |
S1 |
p.
|
artikel
|
| 23 |
P.56 Compensation for metabolic dietitians practicing in North America: Genetic Metabolic Dietitians International 2023 Professional Status Survey
|
Viau, K
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|
141 |
S1 |
p.
|
artikel
|
| 24 |
P.2 Decompensation post-liver transplant in methylmalonic acidemia: a case report
|
Arduini, K
|
|
|
141 |
S1 |
p.
|
artikel
|
| 25 |
P.38 Dietary management in an adverse environment: a case report of GSD III and CGMS
|
Olivares-Sandoval, Z
|
|
|
141 |
S1 |
p.
|
artikel
|
| 26 |
P.25 Diet, growth, body composition and resting energy expenditure in propionic acidemia
|
Myles, JG
|
|
|
141 |
S1 |
p.
|
artikel
|
| 27 |
P.52 Diet management and monitoring of patients during phase 2 and phase 3 pharmaceutical clinical trials: a systematic review approach
|
McWhorter, N
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|
|
141 |
S1 |
p.
|
artikel
|
| 28 |
P.39 Diet therapy for GSD XV: a rare disorder of glycogen synthesis with variable phenotype
|
Pendyal, S
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|
141 |
S1 |
p.
|
artikel
|
| 29 |
P.15 Early management and significant protein restriction in male severe ornithine transcarbamylase deficiency (OTC): a case study
|
Brockett, J
|
|
|
141 |
S1 |
p.
|
artikel
|
| 30 |
P.37 Eating disorders in patients with glycogen storage disease
|
Mount, M
|
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|
141 |
S1 |
p.
|
artikel
|
| 31 |
P.41 Energy utilization issues in multiple acyl-CoA dehydrogenase deficiency type II (severe neonatal onset)
|
Bannister, EN
|
|
|
141 |
S1 |
p.
|
artikel
|
| 32 |
P.12 Enhancing psychosocial support through storytelling: understanding the challenges of women with phenylketonuria and maple syrup urine disease
|
Gurung, SR
|
|
|
141 |
S1 |
p.
|
artikel
|
| 33 |
P.31 Estimating energy needs after pegvaliase response in adults with phenylketonuria
|
Schoen, MS
|
|
|
141 |
S1 |
p.
|
artikel
|
| 34 |
P.6 Evaluation of UCD Anamix Infant as a nutritionally safe and tolerable option for infants with confirmed UCD
|
Burfield, J S
|
|
|
141 |
S1 |
p.
|
artikel
|
| 35 |
P.50 Exploration and development of a mentorship program for metabolic dietitians: The journey of one committee
|
Kopesky, JJ
|
|
|
141 |
S1 |
p.
|
artikel
|
| 36 |
P.9 Findings of a patient registry for MSUD using coordination of rare diseases at Sanford (CoRDS)
|
Dolins, K
|
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|
141 |
S1 |
p.
|
artikel
|
| 37 |
P.22 Hyperammonemia, hypocarnitinemia, rhabdomyolysis and pancreatitis in a patient with undiagnosed 3-methylcrotonyl-CoA carboxylase deficiency
|
McGowan, R
|
|
|
141 |
S1 |
p.
|
artikel
|
| 38 |
P.3 Hyperglycinemia in pediatric patients with propionic acidemia: a review of literature
|
Bertelsmann, C
|
|
|
141 |
S1 |
p.
|
artikel
|
| 39 |
P.26 Impact of arginine-fortified formula on lysine levels in GA1 siblings: a case report
|
Noh, GS
|
|
|
141 |
S1 |
p.
|
artikel
|
| 40 |
P.46 Impact of education for dietitians on dosing and administration of triheptanoin for long-chain fatty acid oxidation disorders
|
Thompson, A
|
|
|
141 |
S1 |
p.
|
artikel
|
| 41 |
P.34 Impact of free amino acids, glycomacropeptide and slow-release protein substitutes on oxidative and inflammatory status in human intestinal Caco-2 cells
|
Tosi, M
|
|
|
141 |
S1 |
p.
|
artikel
|
| 42 |
P.27 Impact of fruit and vegetable protein vs. milk protein on metabolic control of children with phenylketonuria: a randomized crossover controlled trial and 6 months follow-up
|
Pinto, A
|
|
|
141 |
S1 |
p.
|
artikel
|
| 43 |
P.55 Innovation in metabolic nutrition: COVID-19 outreach to support patients on a low protein diet
|
Stelle, EM
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|
141 |
S1 |
p.
|
artikel
|
| 44 |
P.13 Insights from a US and Canada patient and dietitian survey on PKU Sphere®
|
Harrington, M
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|
|
141 |
S1 |
p.
|
artikel
|
| 45 |
P.32 Introducing food allergens to infants with amino acid disorders using a clinic guide and supportive patient educational materials
|
Suares, C
|
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|
141 |
S1 |
p.
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artikel
|
| 46 |
P.43 Ketone supplementation before exercise in long-chain fatty acid oxidation disorder (LC-FAOD) patients suppressed lipolysis despite mild increases in blood ketones
|
Gregor, AN
|
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|
141 |
S1 |
p.
|
artikel
|
| 47 |
P.10 Latest results from the COMPOSE® Phase 1/2 trial of pegtibatinase, a novel investigational enzyme replacement therapy for classical homocystinuria (HCU)
|
Ganesh, J
|
|
|
141 |
S1 |
p.
|
artikel
|
| 48 |
P.1 Management of gestational diabetes in maternal phenylketonuria
|
Arduini, K
|
|
|
141 |
S1 |
p.
|
artikel
|
| 49 |
P.4 Managing a MSUD metabolic crisis and concurrent refeeding syndrome: a case study
|
Bognar, A
|
|
|
141 |
S1 |
p.
|
artikel
|
| 50 |
P.33 Novel dietary management strategies for classical homocystinuria (HCU) in HARMONY/ENSEMBLE phase 3 studies of pegtibatinase, an investigational enzyme replacement therapy
|
Thomas, J
|
|
|
141 |
S1 |
p.
|
artikel
|
| 51 |
P.16 Novel tool for dietary management and monitoring in clinical trials of pegtibatinase, an investigational enzyme replacement therapy for classical homocystinuria
|
Jurecki, E
|
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|
141 |
S1 |
p.
|
artikel
|
| 52 |
P.40 Nutritional changes after an AAV8-mediated liver-directed gene therapy in adults with glycogen storage disease type Ia (GSD Ia)
|
Saavedra, H
|
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|
141 |
S1 |
p.
|
artikel
|
| 53 |
Poster list by author
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|
|
|
141 |
S1 |
p.
|
artikel
|
| 54 |
P.21 Palynziq in a newly incarcerated patient with phenylketonuria (PKU): a case study
|
McDermott, EM
|
|
|
141 |
S1 |
p.
|
artikel
|
| 55 |
P.44 Patient and provider virtual summit: the current state of medium chain acyl-CoA dehydrogenase deficiency management
|
Gurung, SR
|
|
|
141 |
S1 |
p.
|
artikel
|
| 56 |
P.35 Phenylalanine-free infant formula in patients with phenylketonuria: a retrospective study
|
Nas, O Yilmaz
|
|
|
141 |
S1 |
p.
|
artikel
|
| 57 |
P.8 PKU slaaay
|
Daly, A
|
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|
141 |
S1 |
p.
|
artikel
|
| 58 |
Program for the 2024 GMDI Educational Conference
|
|
|
|
141 |
S1 |
p.
|
artikel
|
| 59 |
P.48 Severe variant for pyridoxine dependent epilepsy found in the Micronesian population: a case study
|
Sliwoski, L
|
|
|
141 |
S1 |
p.
|
artikel
|
| 60 |
P.17 Successful outcomes with continued pegvaliase-pqpz treatment throughout pregnancy and lactation in a PKU patient
|
Kopesky, JJ
|
|
|
141 |
S1 |
p.
|
artikel
|
| 61 |
P.53 The effect of the Covid-19 pandemic on weight change and body mass index in children with inborn errors of metabolism
|
Nagy, L
|
|
|
141 |
S1 |
p.
|
artikel
|
| 62 |
P.23 The National PKU Patient Registry: highlighting the methods of phenylketonuria diet management in the United States
|
McQueen, KA
|
|
|
141 |
S1 |
p.
|
artikel
|
| 63 |
P.49 Uncommon rare disease nutrition management: hypokalemic periodic paralysis
|
Arduini, KJ
|
|
|
141 |
S1 |
p.
|
artikel
|
| 64 |
P.19 Use of plant-based peptide formula in patients with organic acidemias
|
Kozek, A
|
|
|
141 |
S1 |
p.
|
artikel
|
| 65 |
P.45 Use of soluble fiber to mitigate gastrointestinal side effects of triheptanoin: a case report
|
Mickle, NK
|
|
|
141 |
S1 |
p.
|
artikel
|
| 66 |
P.20 Utilizing the BioPKU database to personalize nutrition and treatment interventions for patients with PKU
|
Malik, AN
|
|
|
141 |
S1 |
p.
|
artikel
|
| 67 |
Table of Contents
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|
|
|
141 |
S1 |
p.
|
artikel
|
| 68 |
Title Page
|
|
|
|
141 |
S1 |
p.
|
artikel
|
| 69 |
Welcome Letter
|
Hollander, Suzanne
|
|
|
141 |
S1 |
p.
|
artikel
|
Tijdschrift beschrijving