Αποτελέσματα αναζήτησης - Parvaneh, Nima
- Εμφανίζονται 1 - 20 Αποτελέσματα από 38
- Μετάβαση στην Επόμενη Σελίδα
-
1
-
2
-
3
-
4
-
5
Identification of a New Variant in NLRP3 Gene by Whole Exome Sequencing in a Patient with Cryopyrin-Associated Periodic Syndrome από Vahedi, Mahdieh, Parvaneh, Nima, Vahedi, Saeedeh, Shahrooei, Mohammad, Ziaee, Vahid
Έκδοση 2021Κείμενο -
6
-
7
-
8
-
9
-
10
-
11
Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations από Tavasoli, Ali Reza, Parvaneh, Nima, Ashrafi, Mahmoud Reza, Rezaei, Zahra, Zschocke, Johannes, Rostami, Parastoo
Έκδοση 2018Κείμενο -
12
Bacillus Calmette–Guérin (BCG)‐associated hemophagocytic lymphohistiocytosis in the setting of IFN‐γR1 deficiency: A diagnostic dilemma από Razaghian, Anahita, Parvaneh, Leila, Delkhah, Mona, Abbasi, Arash, Sadeghirad, Parisa, Shahrooei, Mohammad, Parvaneh, Nima
Έκδοση 2020Κείμενο -
13
-
14
Effects of Coronavirus Disease 2019 (COVID-19) on Peripheral Blood Lymphocytes and Their Subsets in Children: Imbalanced CD4(+)/CD8(+) T Cell Ratio and Disease Severity από Mahmoudi, Shima, Yaghmaei, Bahareh, Sharifzadeh Ekbatani, Meisam, Pourakbari, Babak, Navaeian, Amene, Parvaneh, Nima, Haghi Ashtiani, Mohammad Taghi, Mamishi, Setareh
Έκδοση 2021Κείμενο -
15
Graft versus host disease and microchimerism in a JAK3 deficient patient από Shahbazi, Zahra, Parvaneh, Nima, Shahbazi, Shirin, Rahimi, Hamzeh, Hamid, Mohammad, Shahbazi, Davoud, Delavari, Samaneh, Abolhassani, Hassan, Aghamohammadi, Asghar, Mahdian, Reza
Έκδοση 2019Κείμενο -
16
Timing of puberty in Iranian girls according to their living area: a national study από Motlagh, Mohammad-Esmaeil, Rabbani, Ali, Kelishadi, Roya, Mirmoghtadaee, Parisa, Shahryari, Safiyeh, Ardalan, Gelayol, Ziaodini, Hassan, Parvaneh, Nima, Khodaei, Shahnaz, Poursafa, Parinaz, Sotoudeh, Aria
Έκδοση 2011Κείμενο -
17
DOCK8 deficiency in six Iranian patients από 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
Έκδοση 2016Κείμενο -
18
Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential RAB27A Effector Engagement από Ohishi, Yuta, Ammann, Sandra, Ziaee, Vahid, Strege, Katharina, Groß, Miriam, Amos, Carla Vazquez, Shahrooei, Mohammad, Ashournia, Parisa, Razaghian, Anahita, Griffiths, Gillian M., Ehl, Stephan, Fukuda, Mitsunori, Parvaneh, Nima
Έκδοση 2020Κείμενο -
19
Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance από Vahidnezhad, Hassan, Youssefian, Leila, Saeidian, Amir Hossein, Ziaee, Vahid, Mahmoudi, Hamidreza, Parvaneh, Nima, Ashjaei, Bahar, Shahrokh, Soroush, Kamyab Hesari, Kambiz, Soltani Zangbar, Mohammadsadegh, Yousefi, Mehdi, Zeinali, Sirous, Uitto, Jouni
Έκδοση 2021Κείμενο -
20
Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE... από Setoodeh, Aria, Panjeh-Shahi, Samareh, Bahmani, Fariba, Vand-Rajabpour, Fatemeh, Jalilian, Nazanin, Sayarifard, Fatemeh, Abbasi, Farzaneh, Sayarifard, Azadeh, Rostami, Parastoo, Parvaneh, Nima, Akhavan-Niaki, Haleh, Ahmadifard, Mohamadreza, Tabrizi, Mina
Έκδοση 2022Κείμενο