Cognitive and adaptive functioning after liver transplantation for maple syrup urine disease: a case series.

scientific article

Cognitive and adaptive functioning after liver transplantation for maple syrup urine disease: a case series. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1111/J.1399-3046.2010.01411.X
P932PMC publication ID3050647
P698PubMed publication ID20946191
P5875ResearchGate publication ID47427831

P50authorHeidi M FeldmanQ63979470
Mary Amanda DewQ87012500
Jerry VockleyQ42112236
George MazariegosQ42906177
P2093author name stringD H Morton
A DeVito Dabbs
R B Noll
K A Strauss
D A Shellmer
P2860cites workElective liver transplantation for the treatment of classical maple syrup urine disease.Q46936591
Social outcome in adults with maple syrup urine disease (MSUD).Q48268538
Academic outcome in long-term survivors of pediatric liver transplantationQ48703576
Assessment of psychoeducational outcomes after pediatric liver transplant.Q51945064
Cognitive performance of children who have undergone liver transplantationQ51949070
Mental and motor development, social competence, and growth one year after successful pediatric liver transplantation.Q52066086
Intellectual outcome in children with maple syrup urine disease.Q52236268
Intellectual performance of children with maple syrup urine diseaseQ70587647
Outcome of early and long-term management of classical maple syrup urine diseaseQ71583458
[Advances in the diagnosis and treatment of maple syrup urine disease: experience in Galicia (Spain)]Q81468899
Neuropsychometric outcome predictors for adults with maple syrup urine diseaseQ83120640
Cognitive development following pediatric solid organ transplantationQ37559219
Cognitive function in children who receive organ transplantationQ40745640
Diagnosis and treatment of maple syrup disease: a study of 36 patientsQ44013322
Developmental profile of patients with maple syrup urine diseaseQ45921973
Metabolic correlates of learning disability.Q46020760
Impact of longitudinal plasma leucine levels on the intellectual outcome in patients with classic MSUD.Q46835000
P433issue1
P921main subjectmaple syrup urine diseaseQ402575
liver transplantationQ1368191
P304page(s)58-64
P577publication date2010-10-08
P1433published inPediatric TransplantationQ7159217
P1476titleCognitive and adaptive functioning after liver transplantation for maple syrup urine disease: a case series
P478volume15

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cites work (P2860)
Q48281291A case of classical maple syrup urine disease that was successfully managed by living donor liver transplantation.
Q37333950Achieving the "triple aim" for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence framework
Q37002969Adaptive functioning and its correlates after intestine and liver transplantation
Q37640465Adipose transplant for inborn errors of branched chain amino acid metabolism in mice
Q36733516Biochemical correlates of neuropsychiatric illness in maple syrup urine disease
Q33617530Brain-blood amino acid correlates following protein restriction in murine maple syrup urine disease
Q34222287Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders.
Q92930679Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomes
Q38219782Child and family adjustment following pediatric solid organ transplantation: factors to consider during the early years post-transplant.
Q50717230Cognitive performance in pediatric liver transplant recipients
Q93000066Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism
Q38069846Domino liver transplantation in maple syrup urine disease: a case report and review of the literature.
Q88611012Evaluation of plasma biomarkers of inflammation in patients with maple syrup urine disease
Q95353303Evaluation of the pediatric patient for liver transplantation: 2014 practice guideline by the American Association for the Study of Liver Diseases, American Society of Transplantation and the North American Society for Pediatric Gastroenterology, He
Q53809440Heterozygote to homozygote related living donor liver transplantation in maple syrup urine disease: a case report.
Q36900920Liver transplantation for classical maple syrup urine disease: long-term follow-up in 37 patients and comparative United Network for Organ Sharing experience
Q38185194Liver transplantation for pediatric metabolic disease
Q48964541Living related versus deceased donor liver transplantation for maple syrup urine disease.
Q48002467Maple syrup urine disease (MSUD): a case with long-term follow-up after liver transplantation
Q36703069Neuropsychiatric Symptoms in Inborn Errors of Metabolism: Incorporation of Genomic and Metabolomic Analysis into Therapeutics and Prevention
Q30487009Nutrition management guideline for maple syrup urine disease: an evidence- and consensus-based approach
Q33861034Successful domino liver transplantation in maple syrup urine disease using a related living donor
Q33632216The start of the transplant journey: referral for pediatric solid organ transplantation.
Q37972714Treatable inborn errors of metabolism causing intellectual disability: a systematic literature review.
Q36571556Two consecutive partial liver transplants in a patient with Classic Maple Syrup Urine Disease

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