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Showing articles 0 to 9 of 9 Filter Applied: failure to thrive (Click to remove) 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 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss Neurol 90:e625-e631, Set, K.K.,et al, 2018 A Floppy Child with Failure to Thrive Lancet 366:176, Loma-Sanner,I.,et al, 2005 Melas Syndrome Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025 Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004 Leigh Syndrome: Serial MR Imaging and Clinical Follow-Up AJNR 21:1502-1509, Arii,J. & Tanabe,Y., 2000 Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ Ann Neurol 34:25-31, Koo,B.,et al, 1993 The Cornelia de Lange Syndrome J Pediatr 63:1000-1020, Ptacek,L.J., 1963 Showing articles 0 to 9 of 9