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Titlebook: JIMD Reports - Case and Research Reports, 2012/1; c/o ACB Book 2012 SSIEM and Springer-Verlag Berlin Heidelberg 2012 endocrinology.inherit

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樓主: calcification
21#
發(fā)表于 2025-3-25 05:06:16 | 只看該作者
Glycine and ,-Arginine Treatment Causes Hyperhomocysteinemia in Cerebral Creatine Transporter Deficfinding of severe hyperhomocysteinemia in one of these cases..Five male patients (age range: 12–20; median = 13 years) genetically confirmed of CRTR deficiency, who were treated with oral glycine (200 mg/kg/day) and .-arginine (400 mg/kg/day) twice a day for 9 months. Clinical follow-up was done at
22#
發(fā)表于 2025-3-25 10:44:33 | 只看該作者
23#
發(fā)表于 2025-3-25 15:19:22 | 只看該作者
Gastrointestinal Phenotype of Fabry Disease in a Patient with Pseudoobstruction Syndrome,essive deposition of GL-3 starts early in life, presumably as early as in fetal life. Chronic burning or provoked attacks of excruciating pain in hands and feet in Fabry disease are common in most children as well as GI-symptoms..We describe a case of pediatric Fabry disease with gastrointestinal dy
24#
發(fā)表于 2025-3-25 16:27:29 | 只看該作者
25#
發(fā)表于 2025-3-25 23:58:14 | 只看該作者
The Paradox of Hyperdopaminuria in Aromatic ,-Amino Acid Deficiency Explained, AADC deficiency, dopamine and serotonin deficiency leads to a severe clinical picture with mental retardation, oculogyric crises, hypotonia, dystonia, and autonomic dysregulation. However, despite dopamine deficiency in the central nervous system, urinary dopamine excretion in AADC-deficient patien
26#
發(fā)表于 2025-3-26 01:08:33 | 只看該作者
A Patient with Congenital Generalized Lipodystrophy Due To a Novel Mutation in ,: Indications for S., encoding seipin (CGL2; MIM 269700), ., encoding caveolin1 (CGL3; MIM 612526) or ., encoding polymerase I and transcript release factor (CGL4; MIM 613327). This study aims to investigate the genotype/phenotype relationship and search for a possible pathogenic mechanism in a patient with CGL...: Ca
27#
發(fā)表于 2025-3-26 06:41:05 | 只看該作者
28#
發(fā)表于 2025-3-26 11:53:07 | 只看該作者
29#
發(fā)表于 2025-3-26 12:48:32 | 只看該作者
Epilepsy in Biotinidase Deficiency After Biotin Treatment,vitis, alopecia, and dermatitis. Clinical features normally appear within the first months of life, between two and five. Seizures are one of the most common symptoms in these patients (55%), usually presented as generalized tonic–clonic, and improving within 24 h of biotin treatment. Treatment dela
30#
發(fā)表于 2025-3-26 17:49:35 | 只看該作者
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