msud
1MSUD — maple syrup urine disease * * * maple syrup urine disease …
2MSUD — • maple syrup urine disease …
3MSUD — biomed. abbr. Maple Syrup Urine Disease …
4Maple syrup urine disease (MSUD) — Hereditary disease due to deficiency of an enzyme involved in amino acid metabolism, characterized by urine that smells like maple syrup …
5Maple syrup urine disease — Classification and external resources Isoleucine (pictured above), leucine, and valine are the branched chain amino acids that build up in MSUD. ICD …
6metabolic disease — ▪ pathology Introduction any of the diseases or disorders that disrupt normal metabolism, the process of converting food to energy on a cellular (cell) level. Thousands of enzymes participating in numerous interdependent metabolic pathways… …
7Dentate nucleus — This article is about the dentate nucleus. For other dentate, see Dentate. Brain: Dentate nucleus Sagittal section through right cerebellar hemisphere. The right olive has also been cut sagitally. (Dentate nucleus labeled at top.) Latin nucleus… …
8BCKDHB — Branched chain keto acid dehydrogenase E1, beta polypeptide (maple syrup urine disease), also known as BCKDHB, is a human gene.cite web | title = Entrez Gene: BCKDHB branched chain keto acid dehydrogenase E1, beta polypeptide (maple syrup urine… …
9Maladie du sirop d'érable — Référence MIM 248600 Transmission Récessive Chromosome 19q13.1 q13.2 6p22 p21 1p31 7q31 q32 Gène BCKDHA BCKDHB DBT GCSL …
10Dihidrolipoil deshidrogenasa — Saltar a navegación, búsqueda Estructura 3D de tres unidades de dihidrolipoildeshidrogenasa. PDB 1ZMC …
