Effect of Whole Exome Sequencing in Diagnosis of Inborn Errors of Metabolism and Neurogenetic Disorders

מאת SHAKIBA, Marjan, KERAMATIPOUR, Mohammad
הוצא לאור ב Iran J Child Neurol (2018)

Producing a Mammalian GFP Expression Vector Containing Neomycin Resistance Gene

מאת Izadi, Manizheh, Abiri, Maryam, Keramatipour, Mohammad
יצא לאור 2009

Effect of Embryonic Cerebrospinal Fluid on Proliferation and Differentiation of Neuroprogenitor Cells

מאת Yari, Siamak, Parivar, Kazem, Nabiuni, Mohammad, Keramatipour, Mohammad
יצא לאור 2013

Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin Gene

מאת ENTEZAM, Mona, AMIRFIROOZI, Akbar, TOGHA, Mansoureh, KERAMATIPOUR, Mohammad
הוצא לאור ב Iran J Public Health (2017)

Succinate Dehydrogenase Deficiency: A Treatable Neurometabolic Disorder

מאת KARIMZADEH, Parvaneh, KERAMATIPOUR, Mohammad, KARAMZADE, Arezou, POURBAKHTYARAN, Elham
הוצא לאור ב Iran J Child Neurol (2020)

A Case Series: Congenital Hyperinsulinism

מאת Alaei, Mohammad Reza, Akbaroghli, Susan, Keramatipour, Mohammad, Alaei, Ali
הוצא לאור ב Int J Endocrinol Metab (2016)

SPOAN syndrome: a novel mutation and new ocular findings; a case report

מאת Bazvand, Fatemeh, Keramatipour, Mohammad, Riazi-Esfahani, Hamid, Mahmoudi, Alireza
הוצא לאור ב BMC Neurol (2021)

Functional Analysis of A Novel Splicing Mutation in The Mutase Gene of Two Unrelated Pedigrees

מאת Ahmadloo, Somayeh, Talebi, Saeed, Miryounesi, Mohammad, Pasalar, Parvin, Keramatipour, Mohammad
הוצא לאור ב Cell J (2016)

3‐Hydroxyisobutyryl‐CoA hydrolase deficiency in an Iranian child with novel HIBCH compound heterozygous mutations

מאת Karimzadeh, Parvaneh, Saberi, Mohammad, Sheidaee, Kobra, Nourbakhsh, Mitra, Keramatipour, Mohammad
הוצא לאור ב Clin Case Rep (2019)

Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient

מאת Alaei, Mohammad Reza, Talebi, Saeed, Ghofrani, Mohammad, Taghizadeh, Mohsen, Keramatipour, Mohammad
הוצא לאור ב Iran Biomed J (2016)

Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient

מאת Alaei, Mohammad Reza, Kheirkhahan, Meghdad, Talebi, Saeed, Davoudi-Dehaghani, Elham, Keramatipour, Mohammad
הוצא לאור ב Iran Biomed J (2020)

PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data()

מאת Entezam, Mona, Khatami, Mohammad Reza, Saddadi, Fereshteh, Ayati, Mohsen, Roozbeh, Jamshid, Keramatipour, Mohammad
הוצא לאור ב Kidney Res Clin Pract (2016)

Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome

מאת Bitarafan, Fatemeh, Razmara, Ehsan, Khodaeian, Mehrnoosh, Keramatipour, Mohammad, Kalhor, Alireza, Jafarinia, Ehsan, Garshasbi, Masoud
הוצא לאור ב Mol Genet Genomic Med (2020)

Whole Exome Sequencing Reveals a XPNPEP3 Novel Mutation Causing Nephronophthisis in a Pediatric Patient

מאת Alizadeh, Rasoul, Jamshidi, Sanaz, Keramatipour, Mohammad, Moeinian, Parisa, Hosseini, Rozita, Otukesh, Hasan, Talebi, Saeed
הוצא לאור ב Iran Biomed J (2020)

Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report

מאת Zardadi, Safoura, Rayat, Sima, Doabsari, Maryam Hassani, Alishiri, Aliagha, Keramatipour, Mohammad, Shahri, Zeynab Javanfekr, Morovvati, Saeid
הוצא לאור ב BMC Pediatr (2021)

Analysis of CFTR Gene Mutations in Children with Cystic Fibrosis, First Report from North-East of Iran

מאת Mehdizadeh Hakkak, Atieh, Keramatipour, Mohammad, Talebi, Saeid, Brook, Azam, Tavakol Afshari, Jalil, Raazi, Amin, Kianifar, Hamid Reza
יצא לאור 2013

Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report

מאת RAZIPOUR, Masoumeh, KOOSHAVAR, Daniz, ALAVINEJAD, Elaheh, SAJEDI, Seyede Zahra, MOHAJER, Neda, SETOODEH, Aria, TALEBI, Saeed, KERAMATIPOUR, Mohammad
הוצא לאור ב Iran J Public Health (2017)

A Novel Variant in the PAH Gene Causing Phenylketonuria in an Iranian Pedigree

מאת Alavinejad, Elaheh, Sajedi, Seyede Zahra, Razipour, Masoumeh, Entezam, Mona, Mohajer, Neda, Setoodeh, Aria, Talebi, Saeed, Keramatipour, Mohammad
הוצא לאור ב Avicenna J Med Biotechnol (2017)

A Novel Mutation in SNX10 Gene Causes Malignant Infantile Osteopetrosis

מאת Amirfiroozy, Akbar, Hamidieh, Amir A., Golchehre, Zahra, Rezamand, Azim, Yahyaei, Mahin, Beiranvandi, Fatemeh, Amirfiroozy, Soheyla, Keramatipour, Mohammad
הוצא לאור ב Avicenna J Med Biotechnol (2017)

CRB1-Related Leber Congenital Amaurosis: Reporting Novel Pathogenic Variants and a Brief Review on Mutations Spectrum

מאת Saberi, Mohammad, Golchehre, Zahra, Karamzade, Arezou, Entezam, Mona, Eshaghkhani, Yeganeh, Alavinejad, Elaheh, Khojasteh Jafari, Hassan, Keramatipour, Mohammad
הוצא לאור ב Iran Biomed J (2019)