Výsledky vyhledávání - Darvish, Hossein

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

Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

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

Získat plný text Získat plný text Získat plný text

Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population Autor 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

Získat plný text Získat plný text Získat plný text

Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder Autor 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

Získat plný text Získat plný text Získat plný text

PTRHD1 (C2orf79) mutations lead to autosomal recessive intellectual disability and parkinsonism Autor 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

Získat plný text Získat plný text Získat plný text

Novel Mutations in TACSTD2 Gene in Families with Gelatinous Drop-like Corneal Dystrophy (GDLD) Autor 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

Získat plný text Získat plný text Získat plný text

PRDM12 Is Transcriptionally Active and Required for Nociceptor Function Throughout Life Autor 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

Získat plný text Získat plný text Získat plný text