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1.
Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations. MedStar authors:
  • Burman, Kenneth D
  • Menucci, Maria Belen
PMID:
  • 32084277
Year: 2020
Citation:
  • Journal of Clinical Endocrinology & Metabolism. 105(3), 2020 03 01.
Institution:
  • MedStar Washington Hospital Center
Department:
  • Medicine/Endocrinology
Medline publication type:
  • Journal Article
Form of publication:
  • Journal Article
All authors:
  • Alikasifoglu A, Burman KD, Dumitrescu AM, Fu J, Gonc EN, Kandemir N, Korwutthikulrangsri M, Liao XH, Menucci MB, Sillers L, Weiss RE
2.
Successful percutaneous coronary intervention in a patient with combined deficiency of FV and FVIII due to novel compound heterozygous mutations in LMAN1. MedStar authors:
  • Malkovska, Vera
PMID:
  • 23557496
Citation:
  • Haemophilia. 19(4):607-10, 2013 Jul.
Institution:
  • Washington Cancer Institute
Medline publication type:
  • Case Reports
  • Journal Article
  • Research Support, N.I.H., Extramural
Form of publication:
  • Journal Article
All authors:
  • Lager RA, Liu HH, Malkovska V, Patel AJ, Zhang B
3.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. MedStar authors:
  • Epstein, Stephen E
PMID:
  • 25487149
Citation:
  • Nature. 518(7537):102-6, 2015 Feb 5.
Institution:
  • MedStar Health Research Institute
Medline publication type:
  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
Form of publication:
  • Journal Article
All authors:
  • Abecasis GR, Allayee H, Altshuler D, Angelica Merlini P, Ardissino D, Asselta R, Assimes TL, Auer PL, Bamshad MJ, Boerwinkle E, Burke GL, Carlson CS, Clarke R, Cresci S, Cupples LA, Danesh J, Davies R, DePristo MA, Do R, Donnelly P, Duga S, Epstein SE, Erdmann J, Farlow DN, Farrall M, Folsom AR, Gabriel S, Girelli D, Goel A, Gross M, Guella I, Hamsten A, Hartiala J, Hazen SL, Hechter E, Hegele RA, Heiss G, Herrington DM, Hovingh GK, Huang J, Jackson RD, Johansen CT, Johnson AD, Jorgensen AB, Kastelein JJ, Kathiresan S, Kiezun A, Kleber ME, Kooperberg C, Kraus WE, Lander ES, Lange EM, Lange LA, Li M, Liu Y, Martinelli N, Marz W, McPherson R, NHLBI Exome Sequencing Project, Nickerson DA, Nikpay M, O'Donnell CJ, Olivieri O, Peloso GM, Psaty BM, Rader DJ, Reilly DF, Reilly MP, Reiner AP, Rich SS, Rivas MA, Roberts R, Rossouw JE, Saleheen D, Samani NJ, Schunkert H, Schwartz SM, Shah SH, Siscovick DS, Sivapalaratnam S, Spertus JA, Stewart AF, Stitziel NO, Sunyaev SR, Tang WH, Taylor HA, Tracy RP, Tybjaerg-Hansen A, Wang J, Watkins H, Wilson JG, Won HH, Yin W, Zuk O
4.
SLCO1B1 variants and urine arsenic metabolites in the Strong Heart Family Study. MedStar authors:
  • Umans, Jason G
PMID:
  • 23970802
Year: 2013
Citation:
  • Toxicological Sciences. 136(1):19-25, 2013 Nov.
Institution:
  • MedStar Health Research Institute
Medline publication type:
  • Journal Article
  • Multicenter Study
  • Research Support, N.I.H., Extramural
Form of publication:
  • Journal Article
All authors:
  • Cole SA, Cropp CD, Fallin MD, Francesconi KA, Goessler W, Gribble MO, Haack K, Kao WH, Laston SL, Maccluer JW, Navas-Acien A, Silbergeld EK, Umans JG, Voruganti VS
5.
Pylephlebitis and acute mesenteric ischemia in a young man with inherited thrombophilia and suspected foodborne illness. MedStar authors:
  • Pradka, Sarah P
  • Ricotta, John J
  • Trankiem, Christine T
PMID:
  • 22520365
Citation:
  • Journal of Vascular Surgery. 55(6):1769-72, 2012 Jun.
Institution:
  • MedStar Washington Hospital Center
Department:
  • Surgery/Trauma Surgery
  • Surgery/Vascular Surgery
Medline publication type:
  • Case Reports
  • Journal Article
Form of publication:
  • Journal Article
All authors:
  • Pradka SP, Ricotta JJ, Trankiem CT
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