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Results 1 - 10 of 31 for Nelson syndrome
  1. ... 6. Epub 2019 Dec 23. Citation on PubMed Nelson A, Myers K. Shwachman-Diamond Syndrome. 2008 Jul 17 [updated 2024 Sep 19]. In: ...
  2. ... on PubMed Kerber KA, Jen JC, Lee H, Nelson SF, Baloh RW. A new episodic ataxia syndrome with linkage to chromosome 19q13. Arch Neurol. 2007 ...
  3. ... Tegay D, Ward K, Maughan A, Maughan G, Nelson L, Wang K, Robison R, Lyon GJ. KBG syndrome involving a single-nucleotide duplication in ANKRD11. Cold ...
  4. ... Attree O, Olivos IM, Okabe I, Bailey LC, Nelson DL, Lewis RA, McInnes RR, Nussbaum RL. The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol ...
  5. ... Mella P, Gandellini F, Stewart DM, Zhu Q, Nelson DL, Notarangelo LD, Ochs HD. Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation ...
  6. ... Allergy Clin Immunol. 2014 Apr;133(4):1232. Nelson, Celeste G [added]. Citation on PubMed or Free article on PubMed Central
  7. ... 61. doi: 10.1007/BF02079072. Citation on PubMed Nelson RA, McNamara M, Ellis W, Stein-Wexler R, Moghaddam B, Zwerdling T. Floating-Harbor syndrome and intramedullary spinal cord ganglioglioma: case report and ...
  8. ... Lu Y, Wilson TA, Gautschi I, Shimkets R, Nelson-Williams C, Rossier BC, Lifton RP. A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation ...
  9. ... IA, Braslavsky D, Bergada I, Dell'Angelica EC, Nelson SF, Martinez-Agosto JA, Achermann JC, Vilain E. Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome. Nat Genet. 2012 May 27;44(7):788- ...
  10. ... 13257. Epub 2015 Nov 27. Citation on PubMed Nelson JA, Demarest S, Thomas J, Juarez-Colunga E, Knupp KG. Evolution of Infantile Spasms to Lennox-Gastaut Syndrome: What Is There to Know? J Child Neurol. ...
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