Post-mortem Diagnosis of Heme Oxygenase-1 Deficiency by Whole Exome Sequencing in an Iranian Child

por Tahghighi, Fatemeh, Parvaneh, Nima, Ziaee, Vahid
Publicado 2019

The Effect of Positive Family History of Autoimmunity in Juvenile Idiopathic Arthritis Characteristics; a Case Control Study

por Khani, Mehdi, Ziaee, Vahid, Moradinejad, Mohamad-Hassan, Parvaneh, Nima
Publicado 2013

Periodic Fever and Neutrophilic Dermatosis: Is It Sweet's Syndrome?

por Assari, Raheleh, Ziaee, Vahid, Parvaneh, Nima, Moradinejad, Mohammad-Hassan
Publicado 2014

Successful Treatment of Fungal Osteomyelitis with Voriconazole in a Patient with Chronic Granulomatous Disease

por Mohammadpour, Masoud, Mamishi, Setareh, Oaji, Mahsa, Pourpak, Zahra, Parvaneh, Nima
Publicado 2010

Identification of a New Variant in NLRP3 Gene by Whole Exome Sequencing in a Patient with Cryopyrin-Associated Periodic Syndrome

por Vahedi, Mahdieh, Parvaneh, Nima, Vahedi, Saeedeh, Shahrooei, Mohammad, Ziaee, Vahid
Publicado 2021

The Efficacy of Anti-Tumor Necrosis Factor Therapy in Cryopyrin-Associated Periodic Syndromes: A Report of Two Cases

por Tahghighi, Fatemeh, Vahedi, Mahdieh, Parvaneh, Nima, Shahrooei, Mohammad, Ziaee, Vahid
Publicado 2022

Neonatal Marfan Syndrome: Report of Two Cases

por Ghandi, Yazdan, S.Zanjani, Keyhan, Mazhari-Mousavi, Seyed-Eshagh, Parvaneh, Nima
Publicado 2013

Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo Diseases

por ASHRAFI, Mahmoud Reza, TAVASOLI, Ali Reza, ALIZADEH, Houman, ZARE NOGHABI, Javad, PARVANEH, Nima
Publicado 2017

Complement deficiency in pediatric-onset systemic lupus erythematosus

por Afzali, Parisa, Isaeian, Anna, Sadeghi, Peyman, Moazzami, Bobak, Parvaneh, Nima, Robatjazi, Masoumeh, Ziaee, Vahid
Publicado 2018

Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations

por Tavasoli, Ali Reza, Parvaneh, Nima, Ashrafi, Mahmoud Reza, Rezaei, Zahra, Zschocke, Johannes, Rostami, Parastoo
Publicado 2018

Bacillus Calmette–Guérin (BCG)‐associated hemophagocytic lymphohistiocytosis in the setting of IFN‐γR1 deficiency: A diagnostic dilemma

por Razaghian, Anahita, Parvaneh, Leila, Delkhah, Mona, Abbasi, Arash, Sadeghirad, Parisa, Shahrooei, Mohammad, Parvaneh, Nima
Publicado 2020

Periodic Fever: A Review on Clinical, Management and Guideline for Iranian Patients - Part I

por Ahmadinejad, Zahra, Mansori, Sedigeh, Ziaee, Vahid, Alijani, Neda, Aghighi, Yahya, Parvaneh, Nima, Mordinejad, Mohammad-Hassan
Publicado 2014

TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two cases

por Aslani, Nahid, Asnaashari, Kosar, Parvaneh, Nima, Shahrooei, Mohammad, Sotoudeh-Anvari, Maryam, Shahram, Farhad, Ziaee, Vahid
Publicado 2022

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

por Mahmoudi, Shima, Yaghmaei, Bahareh, Sharifzadeh Ekbatani, Meisam, Pourakbari, Babak, Navaeian, Amene, Parvaneh, Nima, Haghi Ashtiani, Mohammad Taghi, Mamishi, Setareh
Publicado 2021

Graft versus host disease and microchimerism in a JAK3 deficient patient

por Shahbazi, Zahra, Parvaneh, Nima, Shahbazi, Shirin, Rahimi, Hamzeh, Hamid, Mohammad, Shahbazi, Davoud, Delavari, Samaneh, Abolhassani, Hassan, Aghamohammadi, Asghar, Mahdian, Reza
Publicado 2019

Timing of puberty in Iranian girls according to their living area: a national study

por Motlagh, Mohammad-Esmaeil, Rabbani, Ali, Kelishadi, Roya, Mirmoghtadaee, Parisa, Shahryari, Safiyeh, Ardalan, Gelayol, Ziaodini, Hassan, Parvaneh, Nima, Khodaei, Shahnaz, Poursafa, Parinaz, Sotoudeh, Aria
Publicado 2011

A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in Iran

por Asna Ashari, Kosar, Aslani, Nahid, Parvaneh, Nima, Assari, Raheleh, Heidari, Morteza, Fathi, Mohammadreza, Tahghighi Sharabian, Fatemeh, Ronagh, Alireza, Shahrooei, Mohammad, Moafi, Alireza, Rezaei, Nima, Ziaee, Vahid
Publicado 2023

Demographic, clinical, immunological, and molecular features of iranian national cohort of patients with defect in DCLRE1C gene

por Ghadimi, Soodeh, Jamee, Mahnaz, Abolhassani, Hassan, Parvaneh, Nima, Rezaei, Nima, Delavari, Samaneh, Sadeghi-Shabestari, Mahnaz, Tabatabaei, Sedigheh Rafiei, Fahimzad, Alireza, Armin, Shahnaz, Chavoshzadeh, Zahra, Sharafian, Samin
Publicado 2023

DOCK8 deficiency in six Iranian patients

por 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
Publicado 2016

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

por 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
Publicado 2020