Sökresultat - Parvaneh, Nima

Post-mortem Diagnosis of Heme Oxygenase-1 Deficiency by Whole Exome Sequencing in an Iranian Child av Tahghighi, Fatemeh, Parvaneh, Nima, Ziaee, Vahid

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The Effect of Positive Family History of Autoimmunity in Juvenile Idiopathic Arthritis Characteristics; a Case Control Study av Khani, Mehdi, Ziaee, Vahid, Moradinejad, Mohamad-Hassan, Parvaneh, Nima

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Periodic Fever and Neutrophilic Dermatosis: Is It Sweet's Syndrome? av Assari, Raheleh, Ziaee, Vahid, Parvaneh, Nima, Moradinejad, Mohammad-Hassan

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Successful Treatment of Fungal Osteomyelitis with Voriconazole in a Patient with Chronic Granulomatous Disease av Mohammadpour, Masoud, Mamishi, Setareh, Oaji, Mahsa, Pourpak, Zahra, Parvaneh, Nima

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Identification of a New Variant in NLRP3 Gene by Whole Exome Sequencing in a Patient with Cryopyrin-Associated Periodic Syndrome av Vahedi, Mahdieh, Parvaneh, Nima, Vahedi, Saeedeh, Shahrooei, Mohammad, Ziaee, Vahid

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The Efficacy of Anti-Tumor Necrosis Factor Therapy in Cryopyrin-Associated Periodic Syndromes: A Report of Two Cases av Tahghighi, Fatemeh, Vahedi, Mahdieh, Parvaneh, Nima, Shahrooei, Mohammad, Ziaee, Vahid

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Neonatal Marfan Syndrome: Report of Two Cases av Ghandi, Yazdan, S.Zanjani, Keyhan, Mazhari-Mousavi, Seyed-Eshagh, Parvaneh, Nima

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Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo Diseases av ASHRAFI, Mahmoud Reza, TAVASOLI, Ali Reza, ALIZADEH, Houman, ZARE NOGHABI, Javad, PARVANEH, Nima

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A single center 14 years study of infectious complications leading to hospitalization of patients with primary antibody deficiencies av Mamishi, Setareh, Eghbali, Aiden Nasiri, Rezaei, Nima, Abolhassani, Hassan, Parvaneh, Nima, Aghamohammadi, Asghar

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Complement deficiency in pediatric-onset systemic lupus erythematosus av Afzali, Parisa, Isaeian, Anna, Sadeghi, Peyman, Moazzami, Bobak, Parvaneh, Nima, Robatjazi, Masoumeh, Ziaee, Vahid

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Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations av Tavasoli, Ali Reza, Parvaneh, Nima, Ashrafi, Mahmoud Reza, Rezaei, Zahra, Zschocke, Johannes, Rostami, Parastoo

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Bacillus Calmette–Guérin (BCG)‐associated hemophagocytic lymphohistiocytosis in the setting of IFN‐γR1 deficiency: A diagnostic dilemma av Razaghian, Anahita, Parvaneh, Leila, Delkhah, Mona, Abbasi, Arash, Sadeghirad, Parisa, Shahrooei, Mohammad, Parvaneh, Nima

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Periodic Fever: A Review on Clinical, Management and Guideline for Iranian Patients - Part I av Ahmadinejad, Zahra, Mansori, Sedigeh, Ziaee, Vahid, Alijani, Neda, Aghighi, Yahya, Parvaneh, Nima, Mordinejad, Mohammad-Hassan

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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 av Mahmoudi, Shima, Yaghmaei, Bahareh, Sharifzadeh Ekbatani, Meisam, Pourakbari, Babak, Navaeian, Amene, Parvaneh, Nima, Haghi Ashtiani, Mohammad Taghi, Mamishi, Setareh

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Graft versus host disease and microchimerism in a JAK3 deficient patient av Shahbazi, Zahra, Parvaneh, Nima, Shahbazi, Shirin, Rahimi, Hamzeh, Hamid, Mohammad, Shahbazi, Davoud, Delavari, Samaneh, Abolhassani, Hassan, Aghamohammadi, Asghar, Mahdian, Reza

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Timing of puberty in Iranian girls according to their living area: a national study av Motlagh, Mohammad-Esmaeil, Rabbani, Ali, Kelishadi, Roya, Mirmoghtadaee, Parisa, Shahryari, Safiyeh, Ardalan, Gelayol, Ziaodini, Hassan, Parvaneh, Nima, Khodaei, Shahnaz, Poursafa, Parinaz, Sotoudeh, Aria

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DOCK8 deficiency in six Iranian patients av 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

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Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential RAB27A Effector Engagement av 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

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Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance av 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

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Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE... av 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

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