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Clinical manifestations of mitochondrial DNA depletion.
Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Among authors: koenigsberger mr. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728
Melas: an original case and clinical criteria for diagnosis.
Hirano M, Ricci E, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, DiMauro S, Rowland LP. Hirano M, et al. Among authors: koenigsberger mr. Neuromuscul Disord. 1992;2(2):125-35. doi: 10.1016/0960-8966(92)90045-8. Neuromuscul Disord. 1992. PMID: 1422200 Review.
Cerebellar infarction in children.
Chatkupt S, Epstein LG, Rappaport R, Koenigsberger MR. Chatkupt S, et al. Among authors: koenigsberger mr. Pediatr Neurol. 1987 Nov-Dec;3(6):363-6. doi: 10.1016/0887-8994(87)90009-9. Pediatr Neurol. 1987. PMID: 3508085
Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.
Brzustowicz LM, Allitto BA, Matseoane D, Theve R, Michaud L, Chatkupt S, Sugarman E, Penchaszadeh GK, Suslak L, Koenigsberger MR, et al. Brzustowicz LM, et al. Among authors: koenigsberger mr. Am J Hum Genet. 1994 Mar;54(3):482-8. Am J Hum Genet. 1994. PMID: 8116617 Free PMC article.
Absence of linkage between familial neural tube defects and PAX3 gene.
Chatkupt S, Hol FA, Shugart YY, Geurds MP, Stenroos ES, Koenigsberger MR, Hamel BC, Johnson WG, Mariman EC. Chatkupt S, et al. Among authors: koenigsberger mr. J Med Genet. 1995 Mar;32(3):200-4. doi: 10.1136/jmg.32.3.200. J Med Genet. 1995. PMID: 7783169 Free PMC article.
33 results