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Author/Creator Saghafi, Shiva

1. Delayed diagnosis of hereditary angioedema with C1‐inhibitor deficiency in iranian children and adolescents. Issue 3 (20th March 2019)

Authors:
Ayazi, Maryam; Fazlollahi, Mohammad Reza; Mohammadzadeh, Iraj; Fayezi, Abbas; Nabavi, Mohammad; Mahdaviani, Seyed Alireza; Movahedi, Masoud; Heidarzadeh, Marzieh; Saghafi, Shiva; Shokouhi Shoormasti, Raheleh; Mohammadian, Sajedeh; Farkas, Henriette; Pourpak, Zahra
Journal:
Pediatric allergy and immunology
Issue:
Volume 30:Issue 3(2019)
Page Start:
395
Record Type:
Journal Article
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2. DOCK8 deficiency in six Iranian patients. Issue 6 (17th May 2016)

Authors:
Saghafi, Shiva; Pourpak, Zahra; Nussbaumer, Franziska; Fazlollahi, Mohammad Reza; Houshmand, Massoud; Hamidieh, Amir Ali; Bemanian, Mohammad Hassan; Nabavi, Mohammad; Parvaneh, Nima; Grimbacher, Bodo; Moin, Mostafa; Glocker, Cristina
Journal:
Clinical case reports
Issue:
Volume 4:Issue 6(2016)
Page Start:
593
Record Type:
Journal Article
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3. Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations). (2nd January 2022)

Authors:
Nabilou, Susan; Pak, Fatemeh; Alizadeh, Zahra; Fazlollahi, Mohammad Reza; Houshmand, Masoud; Ayazi, Maryam; Mohammadzadeh, Iraj; Bemanian, Mohammad Hasan; Fayezi, Abbas; Nabavi, Mohammad; Saghafi, Shiva; Mohammadian, Sajedeh; Kokhaei, Parviz; Moin, Mostafa; Pourpak, Zahra
Journal:
Immunological investigations
Issue:
Volume 51:Number 1(2022)
Page Start:
170
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗