JIMD reports. Volume 33 /

JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.

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Bibliographic Details
Other Authors Morava, Eva (Editor), Baumgartner, Matthias R. (Editor), Patterson, Marc (Editor), Rahman, Shamima (Editor), Zschocke, Johannes (Editor), Peters, Verena (Editor)
Format Electronic eBook
LanguageEnglish
Published Berlin, Germany : Springer, 2017.
SeriesJIMD reports ; v. 33.
Subjects
Online AccessFull text
ISBN9783662550120
9783662550113
Physical Description1 online resource (vi, 110 pages) : illustrations (some color)

Cover

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245 0 0 |a JIMD reports.  |n Volume 33 /  |c Eva Morava, editor-in-chief ; Matthias Baumgartner, Marc Patterson, Shamima Rahman, Johannes Zschocke, editors ; Verena Peters, managing editor. 
264 1 |a Berlin, Germany :  |b Springer,  |c 2017. 
300 |a 1 online resource (vi, 110 pages) :  |b illustrations (some color) 
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490 1 |a JIMD reports ;  |v volume 33 
505 0 |a Difficulties in Daily Life and Associated Factors, and QoL of Children with Inherited Metabolic Disease and Their Parents in Japan: A Literature Review -- Swallow Prognosis and Follow-Up Protocol in Infantile Onset Pompe Disease -- Clinical and Genetic Characteristics of Romanian Patients with Mucopolysaccharidosis Type II -- Gastrointestinal Health in Classic Galactosemia -- Management of Life-Threatening Tracheal Stenosis and Tracheomalacia in Patients with Mucopolysaccharidoses -- Brain White Matter Integrity Mediates the Relationship Between Phenylalanine Control and Executive Abilities in Children with Phenylketonuria -- The Challenges of a Successful Pregnancy in a Patient with Adult Refsum's Disease due to Phytanoyl-CoA Hydroxylase Deficiency -- Novel Homozygous Missense Mutation in SPG20 Gene Results in Troyer Syndrome Associated with Mitochondrial Cytochrome c Oxidase Deficiency -- Lethal Neonatal LTBL Associated with Biallelic EARS2 Variants: Case Report and Review of the Reported Neuroradiological Features -- Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling -- Peak Jump Power Reflects the Degree of Ambulatory Ability in Patients with Mitochondrial and Other Rare Diseases -- RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy? -- Missed Newborn Screening Case of Carnitine Palmitoyltransferase-II Deficiency -- Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD) -- Erratum to: Missed Newborn Screening Case of Carnitine Palmitoyltransferase-II Deficiency -- Erratum to: Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD). 
506 |a Plný text je dostupný pouze z IP adres počítačů Univerzity Tomáše Bati ve Zlíně nebo vzdáleným přístupem pro zaměstnance a studenty 
520 |a JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. 
504 |a Includes bibliographical references at the end of each chapters. 
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650 0 |a Metabolism, Inborn errors of. 
650 0 |a Metabolism  |x Disorders. 
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700 1 |a Morava, Eva,  |e editor. 
700 1 |a Baumgartner, Matthias R.,  |e editor. 
700 1 |a Patterson, Marc,  |e editor. 
700 1 |a Rahman, Shamima,  |e editor. 
700 1 |a Zschocke, Johannes,  |e editor. 
700 1 |a Peters, Verena,  |e editor. 
776 0 8 |i Printed edition:  |z 9783662550113 
830 0 |a JIMD reports ;  |v v. 33. 
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