- ... me) Comprehensive update posted live 5 May 2003 (cd,jrg) Revision: molecular ... sporadic adult Alexander disease presenting with acute onset, remission and relapse. J ...
- ... duplicates of studies considered in the previous coeliac disease guideline (CG86). ... studies ( Canavan et al., 2011 ; Duerksen et al., 2010 ; Godfrey ...
- ... free article : PMC1773501 ] [ PubMed : 12477758 ] Not About Celiac Disease (CD) - N=12 1. Agostoni M, Fanti L, Gemma ... 1 Not Human – N=1 Not About Celiac Disease (CD) - N=12 Not About Diagnostic Tests - N=150 ...
- ... Disease C10.228.140.163.100.362.375 Canavan Disease C10.228.140.163.100.362.500 Leukodystrophy, ... Alexander Disease C10.228.140.695.625.375 Canavan Disease C10.228.140.695.625.500 Leukodystrophy, Globoid ...
- ... Disease C10.228.140.163.100.362.375...........................................Canavan Disease C10.228.140.163.100.362.500...........................................Leukodystrophy, ...
- ... psychosis. Biallelic pathogenic variants in HEXA are causative. Canavan disease . Neonatal/infantile (severe) Canavan disease is characterized by evidence of developmental delays by ...
- ... topic><topic ><url >https://medlineplus.gov/genetics/condition/canavan-disease</url><title >Canavan disease</title><other_names ><other_name >ACY2 deficiency</other_ ...
- ... Distinguishing the Disorder from Acute Infantile TSD ASPA Canavan disease – ≤6 mos Macrocephaly, head lag, hypotonia, seizures Leukoencephalopathy, ↑ ... Distinguishing the Disorder from Subacute Juvenile TSD ASPA Canavan disease – ≤6 mos Macrocephaly, head lag, hypotonia, seizures Leukoencephalopathy & ↑ ...
- ... Hereditary Central Nervous System Demyelinating Adrenoleukodystrophy Alexander Disease Canavan Disease Leukodystrophy, Globoid Cell Leukodystrophy, Metachromatic Pelizaeus-Merzbacher Disease ...
- ... Comments Not observed in acute infantile SD ASPA Canavan disease ≤6 mos Macrocephaly, head lag, hypotonia, seizures Leukoencephalopathy ... Comment Not observed in subacute juvenile SD ASPA Canavan disease ≤6 mos Macrocephaly, head lag, hypotonia, seizures Leukoencephalopathy ...
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