Author

Tabibian Shadi

Iranian Comprehensive Hemophilia Care Center - Cited by 1,275 - Thrombosis and hemostasis - Hemophilia - bleeding disorders - Coagulation - Rare bleeding disorders

Biography

Tabibian Shadi is from the Hematology Department, Allied Medical School, Tehran University of Medical Sciences, Tehran, Iran. Hematology, PCR, Oncology, DNA Gel Electrophoresis, and Flow Cytometry are doctors area of interests
Title
Cited by
Year
A comprehensive overview of coagulation factor V and congenital factor V deficiency
S Tabibian, Y Shiravand, M Shams, M Safa, MS Gholami, F Heydari, ...Seminars in thrombosis and hemostasis 45 (05), 523-543, 2019201
57
2019
Diagnosis, clinical manifestations and management of rare bleeding disorders in Iran
A Dorgalaleh, SER Alavi, S Tabibian, S Soori, E Moradi, T Bamedi, ...Hematology 22 (4), 224-230, 2017201
45
2017
Patients with congenital bleeding disorders appear to be less severely affected by SARS-CoV-2: is inherited hypocoagulability overcoming acquired hypercoagulability of …
A Dorgalaleh, A Dabbagh, S Tabibian, MR Baghaeipour, M Jazebi, ...Seminars in thrombosis and hemostasis 46 (07), 853-855, 2020202
36
2020
Intracranial hemorrhage: a devastating outcome of congenital bleeding disorders—prevalence, diagnosis, and management, with a special focus on congenital factor XIII deficiency
SER Alavi, M Jalalvand, V Assadollahi, S Tabibian, A DorgalalehSeminars in Thrombosis and Hemostasis 44 (03), 267-275, 2018201
32
2018
Intracranial hemorrhage in congenital bleeding disorders
S Tabibian, H Motlagh, M Naderi, A DorgalalehBlood Coagulation & Fibrinolysis 29 (1), 1-11, 2018201
26
2018
Molecular basis of congenital factor XIII deficiency in Iran
A Dorgalaleh, V Assadollahi, S Tabibian, M ShamsizadehClinical and applied thrombosis/hemostasis (2), 210-216, 2018201
24
2018
A unique factor XIII mutation in southeastern Iran with an unexpectedly high prevalence: Khash factor XIII
A Dorgalaleh, S Tabibian, M Shams, G Majid, M Naderi, A Casini, ...Seminars in thrombosis and hemostasis 45 (01), 043-049, 2019201
15
2019
Inhibitor development in patients with congenital factor VII deficiency, a study on 50 Iranian patients
M Shams, A Dorgalaleh, N Safarian, AH Emami, F Zaker, S Tabibian, ...Blood Coagulation & Fibrinolysis 30 (1), 24-28, 2019201
14
2019
Persistent hiccups in a patient with mild congenital factor V deficiency and COVID-19; clinical and laboratory finding of a rare bleeding disorder.
A Dorgalaleh, A Dabbagh, S Tabibian, M Bahraini, H RafieemehrInt J Lab Hematol, e87-e88, 2021202
12
2021
Von Willebrand disease in Iran: diagnosis and management
A Dorgalaleh, S Tabibian, M Shams, F Ala, G Bahoush, M Jazebi, ...Ann blood 3 (1), 1-, 2018201
11
2018
Pharmacological management of rare coagulation factor deficiencies besides hemophilia
A Dorgalaleh, S Tabibian, MS Hosseini, M ShamsExpert Review of Hematology 13 (8), 8-834, 2020202
11
2020
Inherited Platelet Function Disorders (IPFDs).
A Dorgalaleh, S Tabibian, M ShamsizadehClinical Laboratory 63 (1), 1-13, 2017201
10
2017
Gastrointestinal bleeding in a newborn infant with congenital factor X deficiency and COVID-19â A common clinical feature between a rare disorder and a new, common infection
A Dorgalaleh, MR Baghaipour, S Tabibian, F Ghazizadeh, A Dabbagh, ...International Journal of Laboratory Hematology 42 (6), e277-e279, 2020202
8
2020
Congenital Factor V Deficiency
S Tabibian, A Dorgalaleh, RM CamireCongenital Bleeding Disorders: Diagnosis and Management, 201-21, 20120
8
2018
Molecular genetic analysis of ten unrelated Iranian patients with congenital factor XIII deficiency
A Dorgalaleh, S Tabibian, T Bamedi, GH Tamaddon, M Naderi, ...International Journal of Laboratory Hematology 39 (2), e33-e36, 20120
7
2017
Minimal factor XIII activity level to prevent major spontaneous bleeds: comment
A Dorgalaleh, SH Tabibian, M Safa, M Shams, M NaderiJournal of Thrombosis and Haemostasis 15 (11), 229-2280, 20120
7
2017
Prenatal diagnosis in rare bleeding disorders—An unresolved issue?
S Tabibian, M Shams, M Naderi, A DorgalalehInternational journal of laboratory hematology 40 (3), 241-250, 2018201
7
2018
Burden of congenital factor XIII deficiency in Iran
A Dorgalaleh, H Motlagh, S Tabibian, M NaderiJ Cell Mol Anesth 2 (03), 142-145, 2017201
6
2017
Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations
B Tavasoli, M Safa, A Dorgalaleh, JB Ghasemi, F Rezaei Makhouri, ...International Journal of Laboratory Hematology 42 (5), 19-27, 2020202
6
2020
Genotyping of blood groups in alloimmunized patients with β-thalassemia major by T-ARMS-PCR and multiplex-aso-pcr
MS Gholami, M Shahidi, S Tabibian, M Naderi, A DorgalalehTransfusion and Apheresis Science 0 (1), 102984, 2021202
6
2021

Referred From: https://scholar.google.com/citations?user=QiE0KQQAAAAJ&hl=en

Cited by
Citations 1275
h-index 19
i10-index 35
Open Access Journals