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Author/Creator Shahani, Tina

1. A novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasia. (30th September 2019)

Authors:
Miryounesi, Mohammad; Nikfar, Ali; Changi‐Ashtiani, Majid; Shahrooei, Mohammad; Dinmohammadi, Hossein; Shahani, Tina; Zarvandi, Samira; Bahrami, Tahereh; Momenilandi, Mana; Rokni‐Zadeh, Hassan
Journal:
Annals of human genetics
Issue:
Volume 84:Number 1(2020:Jan.)
Page Start:
102
Record Type:
Journal Article
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2. GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co‐occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease. Issue 7 (22nd May 2019)

Authors:
Kalayinia, Samira; Maleki, Majid; Rokni‐Zadeh, Hassan; Changi‐Ashtiani, Majid; Ahangar, Hassan; Biglari, Alireza; Shahani, Tina; Mahdieh, Nejat
Journal:
Journal of clinical laboratory analysis
Issue:
Volume 33:Issue 7(2019)
Page Start:
n/a
Record Type:
Journal Article
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3. KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole. (April 2021)

Authors:
Fatemi, Nayeralsadat; Ray, Pierre F.; Ramezanali, Fariba; Shahani, Tina; Amiri-Yekta, Amir; Kherraf, Zine-Eddine; Cazin, Caroline; Almadani, Navid; Varkiani, Maryam; Sarmadi, Soheila; Sodeifi, Niloofar; Gourabi, Hamid; Biglari, Alireza; Totonchi, Mehdi
Journal:
European journal of obstetrics, gynecology, and reproductive biology
Issue:
Volume 259(2021)
Page Start:
100
Record Type:
Journal Article
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5. Pro‐haemostatic effect of DDAVP is partially derived through non‐classical (CD14dim/CD16++) monocytes residing the spleen. Issue 1 (7th December 2022)

Authors:
Salarilak, Laleh; Pirdel, Zahra; Dinmohammadi, Hossein; Rokni‐Zadeh, Hassan; Lavend'homme, Renaud; Karimi, Mehran; Jacquemin, Marc; Shahani, Tina
Journal:
Journal of cellular and molecular medicine
Issue:
Volume 27:Issue 1(2023)
Page Start:
30
Record Type:
Journal Article
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