Total colonic aganglionosis in Hirschsprung disease von Moore, Samuel W., MBChB, FRCS, MD(UCT)

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Intronic RET gene variants in Down syndrome–associated Hirschsprung disease in an African population von Moore, Samuel W, Zaahl, Monique G

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Why has butyrylcholinesterase been retained? Structural and functional diversification in a duplicated gene von Johnson, Glynis, Moore, Samuel W.

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Is Hirschsprung disease a purely neurological condition? A study of the Actin G2 smooth muscle gene in Hirschsprung disease von Moore, Samuel W., Maluleke, Twananani, El Hosny, Ayman A.

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Successful Introduction of Fine Needle Aspiration Biopsy for Diagnosis of Pediatric Lymphadenopathy von Sher-Locketz, Candice, Schubert, Pawel T, Moore, Samuel W, Wright, Colleen A

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Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease von Moore, Samuel W, Zaahl, Monique

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HIV exposure does not worsen outcome in stage III necrotizing enterocolitis with current treatment protocols von Arnold, Marion, Moore, Samuel W

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The Leu-Arg-Glu (LRE) adhesion motif in proteins of the neuromuscular junction with special reference to proteins of the carboxylesterase/cholinesterase family von Johnson, Glynis, Moore, Samuel W.

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Thromboembolism and venous thrombosis of the deep veins in surgical children—an increasing challenge? von Tshifularo, Nyawaleni, Arnold, Marion, Moore, Samuel W

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Interaction of acetylcholinesterase with the G4 domain of the laminin α1-chain von Johnson, Glynis, Swart, Chrisna, Moore, Samuel W.

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The carboxylesterase/cholinesterase gene family in invertebrate deuterostomes von Johnson, Glynis, Moore, Samuel W.

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Non-enzymatic developmental functions of acetylcholinesterase - the question of redundancy von Johnson, Glynis, Swart, Chrisna, Moore, Samuel W

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Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2 von Moore, Samuel W, Appfelstaedt, Justus, Zaahl, Monique G

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Identification of a structural site on acetylcholinesterase that promotes neurite outgrowth and binds laminin-1 and collagen IV von Johnson, Glynis, Moore, Samuel W

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A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling von Moore, Samuel W, Zaahl, Monique G

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Human acetylcholinesterase binds to mouse laminin-1 and human collagen IV by an electrostatic mechanism at the peripheral anionic site von Johnson, Glynis, Moore, Samuel W

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The Adhesion Function on Acetylcholinesterase Is Located at the Peripheral Anionic Site von Johnson, Glynis, Moore, Samuel W.

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Necrotizing Enterocolitis in HIV-Exposed and Nonexposed Infants: Clinical Presentation and Histopathological Features von Chokoe, Mmaphuti J., Wright, Colleen A., Bezuidenhout, Juanita, Moore, Samuel W., Smith, Johan

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Investigations into the development of catalytic activity in anti-acetylcholinesterase idiotypic and anti-idiotypic antibodies von Johnson, Glynis, Moore, Samuel W.

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Hepatocellular carcinoma and liver tumors in South African children: A case for increased prevalence von MOORE, Samuel W, MILLAR, Alistair J. W, HADLEY, G. P, LONESCU, Gabriel, KRUGER, Mariana, POOLE, Janet, STONES, David, WAINWRIGHT, Linda, CHITNIS, Milind, WESSELS, Glynn

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