Results 141 to 150 of about 146,739 (334)

PHENOTYPIC STUDY AND MOLECULA ANALYSIS OF VON WILLEBRAND TYPE 1 PATIENTS

Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2006
BACKGROUND & OBJECTIVE: Von willebrand disease (VWD) is the most common bleeding disorder caused by von willbrand factor (VWF) deficiency and autosomal dominance inheritance pattern. It is divided into three types, one and three (quantitative) and type 2
SMB Hashemi Soteh, N Rezaei, A Goodeve
doaj  

Identification of three candidate mutations causing type IIA von Willebrand disease using a rapid, nonradioactive, allele-specific hybridization method [PDF]

, 1993
Aida Inbal, T Englender, Nurit Kornbrot, AM Randi, Giancarlo Castaman, PM Mannucci, J. Evan Sadler   +6 more
openalex   +1 more source

Gaucher disease, state of the art and perspectives

Journal of Internal Medicine, EarlyView.
Abstract Knowledge about Gaucher disease (GD), considered a model for rare diseases, has considerably increased since its discovery. The pathophysiology of this lysosomal disorder is better known, and specific therapies that can control many aspects of the disease have been developed, particularly for the most common form, Type 1 GD.
Fabrice Camou, Marc G. Berger
wiley   +1 more source

von Willebrand factor and von Willebrand disease [published erratum appears in Blood 1988 Mar;71(3):830]

, 1987
ZM Ruggeri, TS Zimmerman
openalex   +1 more source

Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand disease [PDF]

, 1991
Elizabeth W. Murray, AR Giles, PJ Bridge, IR Peake, D Lillicrap   +4 more
openalex   +1 more source

Genetic Susceptibility to Periodontitis

Journal of Periodontal Research, EarlyView.
Aim: The aim of this narrative review was to identify genes carrying risk alleles associated with an increased risk of periodontitis and to place them in a biological context. Methods: The literature was reviewed based on predefined criteria. Results: The identified genes largely fall into functions linking immune response with tissue repair. The genes
Gesa M. Richter, Arne S. Schaefer
wiley   +1 more source

Molecular studies of von Willebrand disease: reduced von Willebrand factor biosynthesis, storage, and release in endothelial cells derived from patients with type I von Willebrand disease [published erratum appears in Blood 1990 Nov 1;76(9):1901] [PDF]

, 1990
Bruce M. Ewenstein, Aida Inbal, J S Pober, RI Handin   +3 more
openalex   +1 more source

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

Journal of Thrombosis and Haemostasis, 2006
J. Sadler, U. Budde, J. Eikenboom, E. Favaloro, F. Hill, L. Holmberg, J. Ingerslev, Christine A. Lee, D. Lillicrap, P. Mannucci, C. Mazurier, D. Meyer, W. Nichols, M. Nishino, I. Peake, F. Rodeghiero, R. Schneppenheim, Z. Ruggeri, A. Srivastava, R. Montgomery, A. Federici   +20 more
semanticscholar   +1 more source

Von Willebrand disease [PDF]

Clinical Medicine, 2007
openaire   +3 more sources

Porphyromonas gingivalis GroEL exacerbates orthotopic allograft transplantation vasculopathy via impairment of endothelial cell function

Molecular Oral Microbiology, EarlyView.
Abstract Orthotopic allograft transplantation (OAT) is a significant approach to addressing organ failure. However, persistent immune responses to the allograft affect chronic rejection, which induces OAT vasculopathy (OATV) and organ failure. Porphyromonas gingivalis can infiltrate remote organs via the bloodstream, thereby intensifying the severity ...
Chien‐Sung Tsai, Chun‐Yao Huang, Yi‐Ting Tsai, Chun‐Ming Shih, Ze‐Hao Lai, Chen‐Wei Liu, Yi‐Wen Lin, Feng‐Yen Lin   +7 more
wiley   +1 more source