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The Evaluation and Management of Methimazole-Induced Agranulocytosis in the Pediatric Patient: A Case Report and Review of the Literature.
Horm Res Paediatr. 2024 Jan 31. doi: 10.1159/000536508. Online ahead of print.
Horm Res Paediatr. 2024.
PMID: 38295777
Ciliary neurotrophic factor genotype does not influence clinical phenotype in amyotrophic lateral sclerosis.
Al-Chalabi A, Scheffler MD, Smith BN, Parton MJ, Cudkowicz ME, Andersen PM, Hayden DL, Hansen VK, Turner MR, Shaw CE, Leigh PN, Brown RH Jr.
Al-Chalabi A, et al. Among authors: scheffler md.
Ann Neurol. 2003 Jul;54(1):130-4. doi: 10.1002/ana.10638.
Ann Neurol. 2003.
PMID: 12838531
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SPTLC1 is mutated in hereditary sensory neuropathy, type 1.
Bejaoui K, Wu C, Scheffler MD, Haan G, Ashby P, Wu L, de Jong P, Brown RH Jr.
Bejaoui K, et al. Among authors: scheffler md.
Nat Genet. 2001 Mar;27(3):261-2. doi: 10.1038/85817.
Nat Genet. 2001.
PMID: 11242106
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