תרומבאסתניה על-שם גלנצמן (Hebrew Wikipedia)

Analysis of information sources in references of the Wikipedia article "תרומבאסתניה על-שם גלנצמן" in Hebrew language version.

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doi.org

dx.doi.org

AT. Nurden, Glanzmann thrombasthenia, Orphanet Journal of Rare Diseases 1, 2006, עמ' 10 doi: 10.1186/1750-1172-1-10
P. J. Newman, U. Seligsohn, S. Lyman, B. S. Coller, The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel, Proceedings of the National Academy of Sciences of the United States of America 88, 1991, עמ' 3160–3164 doi: 10.1073/pnas.88.8.3160
DL. French, BS. Coller, S Usher, R Berkowitz, Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17: Prenatal Diagnosis of Glanzmann Thrombasthenia, British Journal of Haematology 102, 1998, עמ' 582–587 doi: 10.1046/j.1365-2141.1998.00798.x
R. Yatuv, N. Rosenberg, R. Dardik, B. Brenner, Glanzmann thrombasthenia in two Iraqi-Jewish siblings is caused by a novel splice junction mutation in the glycoprotein IIb, Blood Coagulation & Fibrinolysis: An International Journal in Haemostasis and Thrombosis 9, 1998, עמ' 285–288 doi: 10.1097/00001721-199804000-00011
N. Rosenberg, H. Hauschner, H. Peretz, R. Mor-Cohen, A 13-bp deletion in alphaIIb gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia, Journal of Thrombosis and Haemostasis 3, 2005, עמ' 2764–2772 doi: 10.1111/j.1538-7836.2005.01618.x
S Levy-Mendelovich, T Levy, I Budnik, A A Barg, Low Concentrations of Recombinant Factor VIIa May Improve the Impaired Thrombin Generation of Glanzmann Thrombasthenia Patients, Thrombosis and Haemostasis 119, 2019, עמ' 117–127 doi: 10.1055/s-0038-1676348
M. MORFINI, V. JIMÉNEZ-YUSTE, H. EICHLER, R. FISCHER, Pharmacokinetic properties of two different recombinant activated factor VII formulations, Haemophilia 18, 2011, עמ' 431–436 doi: 10.1111/j.1365-2516.2011.02674.x
A. T. Nurden, J. P. Caen, An Abnormal Platelet Glycoprotein Pattern in Three Cases of Glanzmann's Thrombasthenia, British Journal of Haematology 28, 1974, עמ' 253–260 doi: 10.1111/j.1365-2141.1974.tb06660.x

doi.org

AT. Nurden, Glanzmann thrombasthenia, Orphanet Journal of Rare Diseases 1, 2006, עמ' 10 doi: 10.1186/1750-1172-1-10

mcw.edu

glanzmann.mcw.edu

Wilcox D French D, Glanzmann Thrombasthenia Database, Glanzmann Thrombasthenia Database, ‏2018

nih.gov

pubmed.ncbi.nlm.nih.gov

P. J. Newman, U. Seligsohn, S. Lyman, B. S. Coller, The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel, Proceedings of the National Academy of Sciences of the United States of America 88, 1991, עמ' 3160–3164 doi: 10.1073/pnas.88.8.3160
N. Rosenberg, R. Dardik, E. Rosenthal, A. Zivelin, Mutations in the alphaIIb and beta3 genes that cause Glanzmann thrombasthenia can be distinguished by a simple procedure using transformed B-lymphocytes, Thrombosis and Haemostasis 79, 1998, עמ' 244–248
N. Rosenberg, R. Yatuv, Y. Orion, A. Zivelin, Glanzmann thrombasthenia caused by an 11.2-kb deletion in the glycoprotein IIIa (beta3) is a second mutation in Iraqi Jews that stemmed from a distinct founder, Blood 89, 1997, עמ' 3654–3662
R. Yatuv, N. Rosenberg, R. Dardik, B. Brenner, Glanzmann thrombasthenia in two Iraqi-Jewish siblings is caused by a novel splice junction mutation in the glycoprotein IIb, Blood Coagulation & Fibrinolysis: An International Journal in Haemostasis and Thrombosis 9, 1998, עמ' 285–288 doi: 10.1097/00001721-199804000-00011
H. Peretz, N. Rosenberg, S. Usher, E. Graff, Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene, Blood 85, 1995, עמ' 414–420
S Levy-Mendelovich, T Levy, I Budnik, A A Barg, Low Concentrations of Recombinant Factor VIIa May Improve the Impaired Thrombin Generation of Glanzmann Thrombasthenia Patients, Thrombosis and Haemostasis 119, 2019, עמ' 117–127 doi: 10.1055/s-0038-1676348

wiley.com

onlinelibrary.wiley.com

N. Rosenberg, H. Hauschner, H. Peretz, R. Mor-Cohen, A 13-bp deletion in alphaIIb gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia, Journal of Thrombosis and Haemostasis 3, 2005, עמ' 2764–2772 doi: 10.1111/j.1538-7836.2005.01618.x
M. MORFINI, V. JIMÉNEZ-YUSTE, H. EICHLER, R. FISCHER, Pharmacokinetic properties of two different recombinant activated factor VII formulations, Haemophilia 18, 2011, עמ' 431–436 doi: 10.1111/j.1365-2516.2011.02674.x
A. T. Nurden, J. P. Caen, An Abnormal Platelet Glycoprotein Pattern in Three Cases of Glanzmann's Thrombasthenia, British Journal of Haematology 28, 1974, עמ' 253–260 doi: 10.1111/j.1365-2141.1974.tb06660.x

doi.wiley.com

DL. French, BS. Coller, S Usher, R Berkowitz, Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17: Prenatal Diagnosis of Glanzmann Thrombasthenia, British Journal of Haematology 102, 1998, עמ' 582–587 doi: 10.1046/j.1365-2141.1998.00798.x