Amanote Research

Amanote Research

    RegisterSign In

Autosomal Dominant C1149R Von Willebrand Disease: Phenotypic Findings and Their Implications

Haematologica - Italy
doi 10.3324/haematol.2008.003301
Full Text
Open PDF
Abstract

Available in full text

Categories
Hematology
Date

March 13, 2009

Authors
A. Perez-RodriguezA. Garcia-RiveroE. LouresM. F. Lopez-FernandezA. Rodriguez-TrilloJ. Batlle
Publisher

Ferrata Storti Foundation (Haematologica)


Related search

Von Willebrand Disease Lab Diagnosis

Indian Journal of Hematology and Blood Transfusion
Hematology
2015English

Von Willebrand Disease Type 3

2020English

Linkage Mapping and Phenotypic Analysis of Autosomal Dominant Pallister-Hall Syndrome.

Journal of Medical Genetics
Genetics
1997English

TRPP2 and Autosomal Dominant Polycystic Kidney Disease

Biochimica et Biophysica Acta - Molecular Basis of Disease
Molecular MedicineMolecular Biology
2007English

Diagnosis and Management of Von Willebrand Disease

Haemophilia
MedicineGeneticsHematology
1999English

Interstitial Disease of Autosomal Dominant Polycystic Kidney Disease

Journal of Physiology Studies
2014English

Ectopic (Pelvic) Autosomal Dominant Polycystic Kidney Disease

Internal Medicine
Internal MedicineMedicine
2010English

Åland Archipelago: Von Willebrand Disease and Inazo Nitobe

Japanese Journal of Thrombosis and Hemostasis
2020English

Phenotypic Variability in Autosomal Dominant Familial Alzheimer Disease Due to the S170F Mutation of Presenilin-1

Neurodegenerative Diseases
Neurology
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy