Works matching Von Willebrand disease and genetics

Results: 45

Brief Report von Willebrand's disease and psychotic disorders: co-segregation and genetic associations.

Published in:

Bipolar Disorders, 2004, v. 6, n. 2, p. 150, doi. 10.1111/j.1399-5618.2004.00103.x

By:

Lee, Yu‐Sang;
Miller, Mary;
Hassett, Andrea Cortese;
Lee‐Kim, Byung‐Yeon;
Kim, Jung Jin;
Haracznak, Michelle;
Ranade, Swati;
Wood, Joel;
Reddy, Ravinder;
Kupfer, David J;
Bontempo, Franklin;
Nimgaonkar, Vishwajit L

Publication type:

Article

Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease.

Published in:

Genes, 2022, v. 13, n. 6, p. 971, doi. 10.3390/genes13060971

By:

Naveed, Muhammad Asif;
Abid, Aiysha;
Ali, Nadir;
Hassan, Yaqoob;
Amar, Ali;
Javed, Aymen;
Qamar, Khansa;
Mustafa, Ghulam;
Raza, Ali;
Saleem, Umera;
Hussain, Shabbir;
Shakoor, Madiha;
Khaliq, Shagufta;
Mohsin, Shahida

Publication type:

Article

Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.

Published in:

Indian Journal of Medical Research, 2015, v. 142, n. 6, p. 759, doi. 10.4103/0971-5916.174570

By:

Kasatkar, Priyanka;
Ghosh, Kanjaksha;
Shetty, Shrimati

Publication type:

Article

The Molecular Genetics of von Willebrand Disease.

Published in:

Turkish Journal of Hematology, 2012, v. 29, n. 4, p. 313, doi. 10.5505/tjh.2012.39205

By:

Berber, Ergül

Publication type:

Article

Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients.

Published in:

PLoS ONE, 2018, v. 13, n. 2, p. 1, doi. 10.1371/journal.pone.0192024

By:

Manderstedt, Eric;
Lind-Halldén, Christina;
Lethagen, Stefan;
Halldén, Christer

Publication type:

Article

Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses.

Published in:

Annals of Laboratory Medicine, 2019, v. 39, n. 6, p. 545, doi. 10.3343/alm.2019.39.6.545

By:

Hee-Jung Kim;
Soon Ki Kim;
Ki-Young Yoo;
Ki-O Lee;
Jae Won Yun;
Sun-Hee Kim;
Hee-Jin Kim;
Sang Kyu Park

Publication type:

Article

Genetic variants of VWF gene in type 2 von Willebrand disease.

Published in:

Haemophilia, 2019, v. 25, n. 2, p. e78, doi. 10.1111/hae.13714

By:

Freitas, Samuel da Silva;
Rezende, Suely Meireles;
de Oliveira, Luciana Correa;
Prezotti, Alessandra Nunes Loureiro;
Renni, Marília Sande;
Corsini, Camila Amormino;
Amorim, Marcos Vinícius de Almeida;
Matosinho, Carolina Guimarães Ramos;
Carvalho, Maria Raquel Santos;
Chaves, Daniel Gonçalves

Publication type:

Article

Laboratory aspects of von Willebrand disease: test repertoire and options for activity assays and genetic analysis.

Published in:

Haemophilia, 2014, v. 20, p. 65, doi. 10.1111/hae.12410

By:

CASTAMAN, G.;
HILLARP, A.;
GOODEVE, A.

Publication type:

Article

Laboratory aspects of von Willebrand disease: test repertoire and options for activity assays and genetic analysis.

Published in:

Haemophilia, 2014, v. 20, p. 65, doi. 10.1111/hae.12410

By:

Castaman, G.;
Hillarp, A.;
Goodeve, A.

Publication type:

Article

Patients’ and their family members’ understanding of the genetics of type 1 von Willebrand disease.

Published in:

2008

By:

LANKE, E;
LANKE, J;
LETHAGEN, S

Publication type:

Letter

The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors’ Organisation Haemophilia Genetics Laboratory Network.

Published in:

Haemophilia, 2008, v. 14, n. 5, p. 1099, doi. 10.1111/j.1365-2516.2008.01813.x

By:

KEENEY, S.;
BOWEN, D.;
CUMMING, A.;
ENAYAT, S.;
GOODEVE, A.;
HILL, M.

Publication type:

Article

The inheritance and molecular genetics of von Willebrand's disease.

Published in:

Haemophilia, 1995, v. 1, n. 2, p. 77, doi. 10.1111/j.1365-2516.1995.tb00045.x

By:

Eikenboom, Jeroen C. J.;
Reitsma, Pieter H.;
Briët, Ernest

Publication type:

Article

von Willebrand disease type 2B must be always considered in the differential diagnosis of genetic thrombocytopenias with giant platelets.

Published in:

Platelets, 2006, v. 17, n. 3, p. 149, doi. 10.1080/09537100500441150

By:

Loffredo, Giuseppe;
Baronciani, Luciano;
Noris, Patrizia;
Menna, Francesco;
Federici, Augusto B.;
Balduini, Carlo L.

Publication type:

Article

Genetic Testing for the Diagnosis of Von Willebrand Disease: Benefits and Limitations.

Published in:

Journal of Coagulation Disorders, 2010, v. 2, n. 2, p. 37

By:

Favaloro, Emmanuel J.;
Krigstein, Michael;
Koutts, Jerry;
Brighton, Timothy;
Lindeman, Robert

Publication type:

Article

Association between Genetic Polymorphism and Risk of von Willebrand Disease in Pakistan.

Published in:

BioMed Research International, 2017, v. 2017, p. 1, doi. 10.1155/2017/1070471

By:

Arshad, Najma;
Nawaz, Syed Kashif;
Iqbal, Riffat;
Arshad, Muhammad;
Musheer, Farhana;
Naz, Amber;
Mushtaq, Iqra;
Jaleel, Sara

Publication type:

Article

Características clínicas y diagnóstico genético de la Enfermedad de von Willebrand. Una revisión narrativa.

Published in:

Casos & Revisiones de Salud, 2023, v. 5, n. 2, p. 75, doi. 10.22201/fesz.26831422e.2023.5.2.7

By:

Lizbeth Ávila-Vázquez, Dulce;
Gómez-Villalobos, Guadalupe;
Figueroa-González, Gabriela

Publication type:

Article

Genetic Heterogeneity in a Large Cohort of Indian Type 3 von Willebrand Disease Patients.

Published in:

PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092575

By:

Kasatkar, Priyanka;
Shetty, Shrimati;
Ghosh, Kanjaksha

Publication type:

Article

Molecular genetics of type 2 von Willebrand disease.

Published in:

2002

By:

Fressinaud, Edith;
Mazurier, Claudine;
Meyer, Dominique

Publication type:

journal article

Population-based prevalence and mutational landscape of von Willebrand disease using large-scale genetic databases.

Published in:

NPJ Genomic Medicine, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41525-023-00375-8

By:

Seidizadeh, Omid;
Cairo, Andrea;
Baronciani, Luciano;
Valenti, Luca;
Peyvandi, Flora

Publication type:

Article

Aggregometry in the diagnosis of hemorrhagiparous syndromes.

Published in:

Oncolog-Hematolog, 2018, n. 44, p. 40, doi. 10.26416/onhe.44.3.2018.2026

By:

Găman, Valeriu;
Lupu, Anca

Publication type:

Article

Bleeding Disorder Basics.

Published in:

Pediatric Nursing, 2004, v. 30, n. 5, p. 402

By:

Curry, Heather

Publication type:

Article

Adenosine diphosphate induces binding of von Willebrand factor to human platelets.

Published in:

Nature, 1982, v. 297, n. 5862, p. 154, doi. 10.1038/297154a0

By:

Fujimoto, Takayoshi;
Hawiger, Jack

Publication type:

Article

Acquired von Willebrand Disease Associated with Mantle Cell Lymphoma.

Published in:

Case Reports in Hematology, 2018, p. 1, doi. 10.1155/2018/7973297

By:

Maas, Dominique;
Laros-van Gorkom, Britta;
Gianotten, Sanne;
Cruijsen, Marjan;
van Heerde, Waander;
Nijziel, Marten

Publication type:

Article

Type 1 von Willebrand Disease in a Pediatric Patient Caused by a Novel Heterozygous Deletion of Exons 1 to 6 of the von Willebrand Factor Gene: A Case Report.

Published in:

Laboratory Medicine, 2023, v. 54, n. 4, p. 434, doi. 10.1093/labmed/lmac138

By:

Lapić, Ivana;
Radić Antolic, Margareta;
Rogić, Dunja;
Dejanović Bekić, Sara;
Coen Herak, Désirée;
Bilić, Ernest;
Zadro, Renata

Publication type:

Article

A common founder mutation p.P2063S in exon 36 of VWF in 11 unrelated Indian von Willebrand disease (VWD) families.

Published in:

2013

By:

Kasatkar, Priyanka;
Ghosh, Kanjaksha;
Shetty, Shrimati

Publication type:

Letter

von Willebrand disease and von Willebrand factor.

Published in:

Haemophilia, 2022, v. 28, p. 11, doi. 10.1111/hae.14547

By:

Sadler, Brooke;
Castaman, Giancarlo;
O'Donnell, James S.

Publication type:

Article

von Willebrand disease and von Willebrand factor.

Published in:

Haemophilia, 2022, v. 28, p. 11, doi. 10.1111/hae.14547

By:

Sadler, Brooke;
Castaman, Giancarlo;
O'Donnell, James S.

Publication type:

Article

Genotyping might help therapeutic decision-making in patients with von Willebrand disease type 2 B.

Published in:

Haemophilia, 2016, v. 22, n. 5, p. e439, doi. 10.1111/hae.12960

By:

Rugeri, L.;
Fretigny, M.;
Dargaud, Y.;
Nougier, C.;
Vinciguerra, C.

Publication type:

Article

Contribution of genetical analysis for diagnosis of von Willebrand’s disease type 2B.

Published in:

2009

By:

Victor, M.;
Rugeri, L.;
Nougier, C.;
Meunier, S.;
Fretigny, M.;
Negrier, C.;
Vinciguerra, C.

Publication type:

Letter

The 80th anniversary of von Willebrand's disease: history, management and research.

Published in:

Haemophilia, 2006, v. 12, n. 6, p. 563, doi. 10.1111/j.1365-2516.2006.01393.x

By:

FEDERICI, A. B.;
BERNTORP, E.;
LEE, C. A.

Publication type:

Article

Genetic diagnosis of haemophilia and other inherited bleeding disorders.

Published in:

Haemophilia, 2006, v. 12, p. 82, doi. 10.1111/j.1365-2516.2006.01263.x

By:

Peyvandi, F.;
Jayandharan, G.;
Chandy, M.;
Srivastava, A.;
Nakaya, S. M.;
Johnson, M. J.;
Thompson, A. R.;
Goodeve, A.;
Garagiola, I.;
Lavoretano, S.;
Menegatti, M.;
Palla, R.;
Spreafico, M.;
Tagliabue, L.;
Asselta, R.;
Duga, S.;
Mannucci, P. M.

Publication type:

Article

The molecular biology of von Willebrand disease.

Published in:

Haemophilia, 1999, v. 5, p. 19, doi. 10.1046/j.1365-2516.1999.0050s2019.x

By:

Ginsburg;
Ginsburg, D.

Publication type:

Article

Clinical utility gene card for: von Willebrand disease.

Published in:

European Journal of Human Genetics, 2011, v. 19, n. 5, p. 1, doi. 10.1038/ejhg.2010.222

By:

Cumming, Anthony M.;
Keeney, Stephen;
Jenkins, P. Vincent;
Nash, Michael J.;
O'Donnell, James S.

Publication type:

Article

The molecular characterization of von Willebrand disease: good in parts.

Published in:

British Journal of Haematology, 2013, v. 161, n. 2, p. 166, doi. 10.1111/bjh.12249

By:

James, P.D.;
Lillicrap, D.

Publication type:

Article

Study of Kidney Parameters for Patients with Hemophilia and Von Will Brand patients Infected with Hepatitis B and C.

Published in:

Systematic Reviews in Pharmacy, 2020, v. 11, n. 1, p. 23, doi. 10.5530/srp.2020.1.04

By:

AL-HAMADINY, SHAHAD Q.;
ALEIQABI, RAFEL F. J.;
AL ZAMILY, KHALIED Y. Z.;
FARAJ, SAFAA A.

Publication type:

Article

The Physiologic Basis for Therapy of Classic Hemophilia (Factor VIII Deficiency) and Related Disorders.

Published in:

Annals of Internal Medicine, 1967, v. 67, n. 4, p. 856, doi. 10.7326/0003-4819-67-4-856

By:

Shulman, N. Raphael;
Cowan, Dale H.;
Lubre, Eugene L.;
Watkins, Stanley P.;
Marder, Victor J.

Publication type:

Article

Diagnostic and Therapeutic Difficulties in Type 2A von Willebrand Disease: Resolution.

Published in:

Clinical & Applied Thrombosis/Hemostasis, 2006, v. 12, n. 2, p. 237, doi. 10.1177/107602960601200215

By:

Thomas, M. R.;
Cutler, J. A.;
Savidge, G. F.

Publication type:

Article

Advances in the Management of von Willebrand Disease and Hemophilia.

Published in:

MD Conference Express, 2013, v. 13, n. 13, p. 18, doi. 10.1177/155989771313010

By:

Rizzo, Toni

Publication type:

Article

ISTH bleeding assessment tool and platelet function analyzer in children with mild inherited platelet function disorders.

Published in:

European Journal of Haematology, 2024, v. 113, n. 1, p. 54, doi. 10.1111/ejh.14198

By:

Alhaj, Dana;
Hagedorn, Nikola;
Cuntz, Franziska;
Reschke, Madlen;
Schuldes, Joerg;
Ruthenberg, Juliane;
Bakchoul, Tamam;
Greinacher, Andreas;
Holzhauer, Susanne

Publication type:

Article

Von Willebrand disease - the ' Dos' and ' Don'ts' in surgery.

Published in:

European Journal of Haematology, 2017, v. 98, n. 2, p. 121, doi. 10.1111/ejh.12809

By:

Miesbach, Wolfgang;
Berntorp, Erik

Publication type:

Article

Opening Plenary Lectures.

Published in:: 2009
Publication type:: Abstract

Misdiagnosis of type 2B von Willebrand disease as immune thrombocytopenia in a thrombocytopenic patient.

Published in:

2024

By:

Lu, Xiaodong;
Yu, Diao;
Dai, Wenchu;
Zou, Menglan;
Liu, Jinlin

Publication type:

Letter

Factor VIII-von Willebrand Factor Binding Defects in Autosomal Recessive von Willebrand Disease Type Normandy and in Mild Hemophilia A.

Published in:

Acta Haematologica, 2009, v. 121, n. 2/3, p. 102, doi. 10.1159/000214849

By:

Jacquemin, Marc

Publication type:

Article

Von Willebrand Factor 1 and Factor 2 Alleles (Intron 40) Are Suitable Markers for Carrier Detection in von Willebrand Disease Families in the Indian Population.

Published in:

Acta Haematologica, 2006, v. 115, n. 1/2, p. 64, doi. 10.1159/000089468

By:

Trasi, Sucheta;
Mohanty, Dipika;
Pathare, Anil;
Shetty, Shrimati;
Ghosh, Kanjaksha

Publication type:

Article

Alagille syndrome and hereditary von Willebrand disease: A rare co-occurrence.

Published in:

South African Journal of Child Health, 2021, v. 15, n. 3, p. 175, doi. 10.7196/SAJCH.2021.v15.i3.1820

By:

Dempster, M. J.;
Jacobson, B. F.;
Walabh, P.

Publication type:

Article