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Massoud Houshmand

Showing results (131-140 of 161) with videos related to

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Ecology and Evolution|March 7, 2012
Comprehensive study of mtDNA among Southwest Asian dogs contradicts independent domestication of wolf, but implies dog-wolf hybridizationArman Ardalan, Cornelya F C Kluetsch, Ai-Bing Zhang, et al.
Therapeutics and Clinical Risk Management|February 19, 2016
Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing lossMaryam Balali, Behnam Kamalidehghan, Mohammad Farhadi, et al.
Molecular Biology Reports|December 18, 2012
Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing lossMohammad Ali Dowlati, Pupak Derakhshandeh-Peykar, Massoud Houshmand, et al.
Iranian Journal of Allergy, Asthma, and Immunology|July 12, 2026
Clinical Manifestations and Genetic Findings in Three Patients with Chediak-Higashi Syndrome: Highlighting the Splice Site VariantsShaghayegh Tajik, Anne Molitor, Zahra Alizadeh, et al.
BMC Research Notes|August 30, 2012
Specific-mutational patterns of p53 gene in bladder transitional cell carcinoma among a group of Iraqi patients exposed to war environmental hazardsThekra A Al-Kashwan, Massoud Houshmand, Asaad Al-Janabi, et al.
Iranian Journal of Allergy, Asthma, and Immunology|April 1, 2023
The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD ChildSeyedeh Zalfa Modarresi, Shagayegh Tajik, Mohsen Badalzadeh, et al.
Biochemical Genetics|October 18, 2021
Following the Trace of HVS II Mitochondrial Region Within the Nine Iranian Ethnic Groups Based on Genetic Population AnalysisAnousheh Shasttiri, Misagh Moridi, Abbas Safari, et al.
Physiological Reports|January 29, 2015
Complex genetic background in a large family with Brugada syndromeSiamak Saber, Mohamed-Yassine Amarouch, Amir-Farjam Fazelifar, et al.
Iranian Journal of Allergy, Asthma, and Immunology|April 5, 2020
Clinical and Genetic Analysis of Nine Suspected Familial Haemophagocytic Lymphohistiocytosis Patients for MUNC13-4 Deficiency and Introducing Four Novel Mutations in UNC13DMaryam Vahidi, Mohsen Badalzadeh, Masoomeh Jannesar, et al.
Iranian Journal of Allergy, Asthma, and Immunology|July 13, 2022
Confirmation of Hyperimmunoglobulin E Syndrome in Two Patients with an Ocular Problem: Detection of Two New DOCK8 MutationsShiva Saghafi, Fariborz Zandieh, Mohammad Reza Fazlollahi, et al.
Pageof 17

Showing results (131-140 of 161) with videos related to

Sort By:
Pageof 17
Ecology and Evolution|March 7, 2012
Comprehensive study of mtDNA among Southwest Asian dogs contradicts independent domestication of wolf, but implies dog-wolf hybridizationArman Ardalan, Cornelya F C Kluetsch, Ai-Bing Zhang, et al.
Therapeutics and Clinical Risk Management|February 19, 2016
Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing lossMaryam Balali, Behnam Kamalidehghan, Mohammad Farhadi, et al.
Molecular Biology Reports|December 18, 2012
Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing lossMohammad Ali Dowlati, Pupak Derakhshandeh-Peykar, Massoud Houshmand, et al.
Iranian Journal of Allergy, Asthma, and Immunology|July 12, 2026
Clinical Manifestations and Genetic Findings in Three Patients with Chediak-Higashi Syndrome: Highlighting the Splice Site VariantsShaghayegh Tajik, Anne Molitor, Zahra Alizadeh, et al.
BMC Research Notes|August 30, 2012
Specific-mutational patterns of p53 gene in bladder transitional cell carcinoma among a group of Iraqi patients exposed to war environmental hazardsThekra A Al-Kashwan, Massoud Houshmand, Asaad Al-Janabi, et al.
Iranian Journal of Allergy, Asthma, and Immunology|April 1, 2023
The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD ChildSeyedeh Zalfa Modarresi, Shagayegh Tajik, Mohsen Badalzadeh, et al.
Biochemical Genetics|October 18, 2021
Following the Trace of HVS II Mitochondrial Region Within the Nine Iranian Ethnic Groups Based on Genetic Population AnalysisAnousheh Shasttiri, Misagh Moridi, Abbas Safari, et al.
Physiological Reports|January 29, 2015
Complex genetic background in a large family with Brugada syndromeSiamak Saber, Mohamed-Yassine Amarouch, Amir-Farjam Fazelifar, et al.
Iranian Journal of Allergy, Asthma, and Immunology|April 5, 2020
Clinical and Genetic Analysis of Nine Suspected Familial Haemophagocytic Lymphohistiocytosis Patients for MUNC13-4 Deficiency and Introducing Four Novel Mutations in UNC13DMaryam Vahidi, Mohsen Badalzadeh, Masoomeh Jannesar, et al.
Iranian Journal of Allergy, Asthma, and Immunology|July 13, 2022
Confirmation of Hyperimmunoglobulin E Syndrome in Two Patients with an Ocular Problem: Detection of Two New DOCK8 MutationsShiva Saghafi, Fariborz Zandieh, Mohammad Reza Fazlollahi, et al.
Pageof 17