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Nima Parvaneh

Showing results (51-60 of 161) with videos related to

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Iranian Journal of Pediatrics|March 21, 2015
Periodic Fever: a review on clinical, management and guideline for Iranian patients - part IZahra Ahmadinejad, Sedigeh Mansori, Vahid Ziaee, et al.
Iranian Journal of Allergy, Asthma, and Immunology|February 22, 2025
How Hospitalizations Can Be Effective in Subsequent Care of Children with Asthma?Samin Sharafian, Ghasem Barjouei Fard, Maryam Atabakzadeh, et al.
European Journal of Medical Genetics|February 29, 2012
2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delayAli Rashidi-Nezhad, Nima Parvaneh, Farideh Farzanfar, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 11, 2008
Pubertal development in a random sample of 4,020 urban Iranian girlsAli Rabbani, Shahnaz Khodai, Kazem Mohammad, et al.
Immunological Investigations|December 4, 2013
Combined immunodeficiency presenting with vaccine-associated paralytic poliomyelitis: a case report and narrative review of literatureMohammadreza Shaghaghi, Nima Parvaneh, Pouya Ostad-Rahimi, et al.
British Journal of Haematology|April 22, 2008
Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous diseaseShahram Teimourian, Elham Zomorodian, Mohsen Badalzadeh, et al.
BMC Pediatrics|April 24, 2025
Safety of MMR vaccination evaluated in children with food and gelatin allergy in IranMehdi Shokri, Masoud Movahedi, Nima Parvaneh, et al.
Acta Dermatovenerologica Croatica : ADC|January 16, 2013
Epidermodysplasia verruciformis associated with plasmablastic lymphoma and hepatitis B virus infectionNasrin Shayanfar, Pegah Babaheidarian, Hoda Rahmani, et al.
Annals of Hepatology|October 21, 2009
Evaluation of liver diseases in Iranian patients with primary antibody deficienciesFarzaneh Motamed, Asghar Aghamohammadi, Mahmoud Soltani, et al.
Pigment Cell & Melanoma Research|April 8, 2010
Functional characterization of two RAB27A missense mutations found in Griscelli syndrome type 2Norihiko Ohbayashi, Setareh Mamishi, Koutaro Ishibashi, et al.
Pageof 17

Showing results (51-60 of 161) with videos related to

Sort By:
Pageof 17
Iranian Journal of Pediatrics|March 21, 2015
Periodic Fever: a review on clinical, management and guideline for Iranian patients - part IZahra Ahmadinejad, Sedigeh Mansori, Vahid Ziaee, et al.
Iranian Journal of Allergy, Asthma, and Immunology|February 22, 2025
How Hospitalizations Can Be Effective in Subsequent Care of Children with Asthma?Samin Sharafian, Ghasem Barjouei Fard, Maryam Atabakzadeh, et al.
European Journal of Medical Genetics|February 29, 2012
2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delayAli Rashidi-Nezhad, Nima Parvaneh, Farideh Farzanfar, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 11, 2008
Pubertal development in a random sample of 4,020 urban Iranian girlsAli Rabbani, Shahnaz Khodai, Kazem Mohammad, et al.
Immunological Investigations|December 4, 2013
Combined immunodeficiency presenting with vaccine-associated paralytic poliomyelitis: a case report and narrative review of literatureMohammadreza Shaghaghi, Nima Parvaneh, Pouya Ostad-Rahimi, et al.
British Journal of Haematology|April 22, 2008
Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous diseaseShahram Teimourian, Elham Zomorodian, Mohsen Badalzadeh, et al.
BMC Pediatrics|April 24, 2025
Safety of MMR vaccination evaluated in children with food and gelatin allergy in IranMehdi Shokri, Masoud Movahedi, Nima Parvaneh, et al.
Acta Dermatovenerologica Croatica : ADC|January 16, 2013
Epidermodysplasia verruciformis associated with plasmablastic lymphoma and hepatitis B virus infectionNasrin Shayanfar, Pegah Babaheidarian, Hoda Rahmani, et al.
Annals of Hepatology|October 21, 2009
Evaluation of liver diseases in Iranian patients with primary antibody deficienciesFarzaneh Motamed, Asghar Aghamohammadi, Mahmoud Soltani, et al.
Pigment Cell & Melanoma Research|April 8, 2010
Functional characterization of two RAB27A missense mutations found in Griscelli syndrome type 2Norihiko Ohbayashi, Setareh Mamishi, Koutaro Ishibashi, et al.
Pageof 17