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Showing articles 0 to 6 of 6 Filter Applied: failure to thrive (Click to remove) Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss Neurol 90:e625-e631, Set, K.K.,et al, 2018 Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification NEJM 313:139-181, Sly,W.S.,et al, 1985 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018 Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004 Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998 Showing articles 0 to 6 of 6