Søgeresultater - Darvish, Hossein

A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney Disease af Jamshidi, Javad, Naderi, Hamed, Taghavi, Shaghayegh, Emamalizadeh, Babak, Darvish, Hossein

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XRCC1 and OGG1 Gene Polymorphisms and Breast Cancer: A Systematic Review of Literature af Sanjari Moghaddam, Ali, Nazarzadeh, Milad, Noroozi, Rezvan, Darvish, Hossein, Mosavi Jarrahi, Alireza

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Emery-Dreifuss Muscular Dystrophy: a Report of a Large Family with 11 Affected Individuals af Ahmadifard, Azadeh, Jamshidi, Javad, Tafakhori, Abbas, Mollazadeh, Reza, Falsafi, Zeinab, Darvish, Hossein

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Clinical and molecular spectrum of P/Q type calcium channel Cav2.1 in epileptic patients af Alehabib, Elham, Esmaeilizadeh, Zahra, Ranji-Burachaloo, Sakineh, Tafakhori, Abbas, Darvish, Hossein, Movafagh, Abolfazl

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Whole genome sequencing identifies a novel homozygous exon deletion in the NT5C2 gene in a family with intellectual disability and spastic paraplegia af Darvish, Hossein, Azcona, Luis J., Tafakhori, Abbas, Ahmadi, Mona, Ahmadifard, Azadeh, Paisán-Ruiz, Coro

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FABP9 Mutations Are Not Detected in Cases of Infertility due to Sperm Morphological Defects in Iranian Men af Jamshidi, Javad, Pouresmaeili, Farkhondeh, Darvish, Hossein, Omrani, Mir Davood, Azargashb, Eznollah, Sadeghi, Mohammad Reza, Lakpour, Niknam

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Molecular characterization of PRKN structural variations identified through whole‐genome sequencing af Bravo, Paloma, Darvish, Hossein, Tafakhori, Abbas, Azcona, Luis J., Johari, Amir Hossein, Jamali, Faezeh, Paisán‐Ruiz, Coro

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Identification of a large homozygous VPS13C deletion in a patient with early-onset parkinsonism af Darvish, Hossein, Bravo, Paloma, Tafakhori, Abbas, Azcona, Luis J., Ranji-Burachaloo, Sakineh, Johari, Amir Hossein, Paisán-Ruiz, Coro

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Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome af Ghaedi, Hamid, Ramsheh, Samira Molaei, Omidvar, Maryam Erfanian, Labbaf, Afsaneh, Alehabib, Elham, Akbari, Sanaz, Pourfatemi, Fatemeh, Darvish, Hossein

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Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism af Sanchez, Elena, Darvish, Hossein, Mesias, Roxana, Taghavi, Shaghyegh, Firouzabadi, Saghar Ghasemi, Walker, Ruth H., Tafakhori, Abbas, Paisán-Ruiz, Coro

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A novel PUS7 mutation causes intellectual disability with autistic and aggressive behaviors af Darvish, Hossein, Azcona, Luis J., Alehabib, Elham, Jamali, Faezeh, Tafakhori, Abbas, Ranji-Burachaloo, Sakineh, Jen, Joanna C., Paisán-Ruiz, Coro

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Genetic screening in two Iranian families with early onset Alzheimer’s disease identified a novel PSEN1 mutation af Wang, Jen-Chyong, Alinaghia, Somayeh, Tafakhori, Abbas, Sikora, Elizabeth, Azcona, Luis J., Karkheiran, Siamak, Goate, Alison, Paisán-Ruiz, Coro, Darvish, Hossein

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Recessive COL4A2 Mutation Leads to Intellectual Disability, Epilepsy, and Spastic Cerebral Palsy af Bakhtiari, Somayeh, Tafakhori, Abbas, Jin, Sheng Chih, Guida, Brandon S., Alehabib, Elham, Firouzbadi, Saghar, Bilguvar, Kaya, Fahey, Michael C., Darvish, Hossein, Kruer, Michael C.

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Monoamine Oxidase A Gene Polymorphisms and Bipolar Disorder in Iranian Population af Eslami Amirabadi, Mohammad Reza, Rajezi Esfahani, Sepideh, Davari-Ashtiani, Rozita, Khademi, Mojgan, Emamalizadeh, Babak, Movafagh, Abolfazl, Sadr, Said, Arabgol, Fariba, Darvish, Hossein, Razjoyan, Katayoon

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No Evidence for Association Between Norepinephrine Transporter-3081 (A/T) Polymorphism and Attention Deficit Hyperactivity Disorder in Iranian Population af Eslami Amirabadi, Mohammad Reza, Davari-Ashtiani, Rozita, Khademi, Mojgan, RajeziEsfahani, Sepideh, Emamalizadeh, Babak, Movafagh, Abolfazl, Arabgol, Fariba, Sadr, Said, Darvish, Hossein, Razjouyan, Katayoon

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Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population af Madadi, Faranak, Khaniani, Mahmoud Shekari, Shandiz, Ehsan Esmaili, Ayromlou, Hormoz, Najmi, Safa, Emamalizadeh, Babak, Taghavi, Shaghayegh, Jamshidi, Javad, Tafakhori, Abbas, Shahidi, Gholam-Ali, Darvish, Hossein

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Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder af Mattioli, Francesca, Darvish, Hossein, Paracha, Sohail Aziz, Tafakhori, Abbas, Firouzabadi, Saghar Ghasemi, Chapi, Marjan, Baig, Hafiz Muhammad Azhar, Reymond, Alexandre, Antonarakis, Stylianos E., Ansar, Muhammad

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PTRHD1 (C2orf79) mutations lead to autosomal recessive intellectual disability and parkinsonism af Khodadadi, Hamidreza, Azcona, Luis J., Aghamollaii, Vajiheh, Omrani, Mir Davood, Garshasbi, Masoud, Taghavi, Shaghayegh, Tafakhori, Abbas, Shahidi, Gholam Ali, Jamshidi, Javad, Darvish, Hossein, Paisán-Ruiz, Coro

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Novel Mutations in TACSTD2 Gene in Families with Gelatinous Drop-like Corneal Dystrophy (GDLD) af Alehabib, Elham, Jamshidi, Javad, Ghaedi, Hamid, Emamalizadeh, Babak, Andarva, Monavvar, Daftarian, Narsis, Rezaei Kanavi, Mozhgan, Mohammadi Torbati, Peyman, Espandar, Goldis, Alinaghi, Somayeh, Johari, Amir Hossein, Saghally, Mansoor, Mohajerani, Fatemeh, Darvish, Hossein

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PRDM12 Is Transcriptionally Active and Required for Nociceptor Function Throughout Life af Kokotović, Tomislav, Langeslag, Michiel, Lenartowicz, Ewelina M., Manion, John, Fell, Christopher W., Alehabib, Elham, Tafakhori, Abbas, Darvish, Hossein, Bellefroid, Eric J., Neely, G. Gregory, Kress, Michaela, Penninger, Josef M., Nagy, Vanja

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