M. Priscilla Short - Publications, H-index & Citations

M. Priscilla Short

机构信息待补充

36H指数

75论文数

7.3K被引数

收录论文 8

发表时间

IMPOWER: a national patient-generated registry for intestinal malrotation exploring diagnosis, treatment, and surgical outcomes

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2023-05-11

OAAI

Martinez, Sydney A.; Fligor, Scott C.; Tsikis, Savas; Short, Meagan; Corcoran, Katie E.; Rogers, Amy; Gura, Kathleen M.; Puder, Mark

Reconsidering the family history in primary care

JOURNAL OF GENERAL INTERNAL MEDICINE

IF4.2

2004-03-01

282

OAAI

Rich, EC; Burke, W; Heaton, CJ; Haga, S; Pinsky, L; Short, MP; Acheson, L

The physician's role in discussing organ donation with families

CRITICAL CARE MEDICINE

IF6

2003-05-01

106

PREAI

Williams, MA; Lipsett, PA; Rushton, CH; Grochowski, EC; Berkowitz, ID; Mann, SL; Shatzer, JH; Short, MP; Genel, M

CT imaging in adults with neurofibromatosis-1 - Frequent asymptomatic plexiform lesions

NEUROLOGY

IF8.5

1998-06-01

122

PREAI

Tonsgard, JH; Kwak, SM; Short, P; Dachman, AH

Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

1997-12-01

141

OAAI

Jacoby, LB; Jones, D; Davis, K; Kronn, D; Short, MP; Gusella, J; MacCollin, M

Human XPMC2H: cDNA cloning, mapping to 9q34, genomic structure, and evaluation as TSC1

GENOMICS

IF3

1997-09-01

PREAI

Kwiatkowska, J; Slomski, R; Jozwiak, S; Short, MP; Kwiatkowski, DJ

Clinical and biochemical manifestations of hyaluronidase deficiency

NEW ENGLAND JOURNAL OF MEDICINE

IF78.5

1996-10-03

146

OAAI

Natowicz, MR; Short, MP; Wang, Y; Dickersin, GR; Gebhardt, MC; Rosenthal, DI; Sims, KB; Rosenberg, AE

Novel mutations detected in the TSC2 gene from both sporadic and familial TSC patients

HUMAN MOLECULAR GENETICS

IF3.2

1996-02-01

OAAI

Wilson, PJ; Ramesh, V; Kristiansen, A; Bove, C; Jozwiak, S; Kwiatkowski, DJ; Short, MP; Haines, JL

研究方向