Works matching AU Najafi, Maryam

Results: 53
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    Higher Glycemic Index and Load Could Increase Risk of Dyslipidemia.

    Published in:
    International Journal of Nutrition Sciences, 2023, v. 8, n. 3, p. 150, doi. 10.30476/IJNS.2023.97742.1219
    By:
    • Soltani, Mitra;
    • Gerami, Shirin;
    • Far, Zohreh Ghaem;
    • Rajabzadeh-Dehkordi, Milad;
    • Dehzad, Mohammad Jafar;
    • Najafi, Maryam;
    • Faghih, Shiva
    Publication type:
    Article
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    MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss.

    Published in:
    Human Genetics, 2018, v. 137, n. 6/7, p. 479, doi. 10.1007/s00439-018-1901-4
    By:
    • Bademci, Guney;
    • Abad, Clemer;
    • Incesulu, Armagan;
    • Rad, Abolfazl;
    • Alper, Ozgul;
    • Kolb, Susanne M.;
    • Cengiz, Filiz B.;
    • Diaz-Horta, Oscar;
    • Silan, Fatma;
    • Mihci, Ercan;
    • Ocak, Emre;
    • Najafi, Maryam;
    • Maroofian, Reza;
    • Yilmaz, Elanur;
    • Nur, Banu G.;
    • Duman, Duygu;
    • Guo, Shengru;
    • Sant, David W.;
    • Wang, Gaofeng;
    • Monje, Paula V.
    Publication type:
    Article
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    Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking.

    Published in:
    2021
    By:
    • Sanderson, Leslie E;
    • Lanko, Kristina;
    • Alsagob, Maysoon;
    • Almass, Rawan;
    • Al-Ahmadi, Nada;
    • Najafi, Maryam;
    • Al-Muhaizea, Mohammad A;
    • Alzaidan, Hamad;
    • AlDhalaan, Hesham;
    • Perenthaler, Elena;
    • Linde, Herma C van der;
    • Nikoncuk, Anita;
    • Kühn, Nikolas A;
    • Antony, Dinu;
    • Owaidah, Tarek Mustafa;
    • Raskin, Salmo;
    • Vieira, Luana Gabriela Dalla Rosa;
    • Mombach, Romulo;
    • Ahangari, Najmeh;
    • Silveira, Tainá Regina Damaceno
    Publication type:
    journal article
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    Anti-Müllerian hormone as a predictor of IVF treatment.

    Published in:
    Tehran University Medical Journal, 2012, v. 70, n. 6, p. 371
    By:
    • Mehrafza, Marzieh;
    • Raoufi, Azadeh;
    • Abdollahian, Parvaneh;
    • Nikpouri, Zahra;
    • Shadmani, Kimia;
    • Najafi, Maryam;
    • Vojoudi, Elham;
    • Hosseini, Ahmad
    Publication type:
    Article
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    The First Inherited Retinal Disease Registry in Iran: Research Protocol and Results of a Pilot Study.

    Published in:
    Archives of Iranian Medicine (AIM), 2020, v. 23, n. 7, p. 445, doi. 10.34172/aim.2020.41
    By:
    • Sabbaghi, Hamideh;
    • Daftarian, Narsis;
    • Suri, Fatemeh;
    • Mirrahimi, Mehraban;
    • Madani, Sina;
    • Sheikhtaheri, Abbas;
    • Khorrami, Farid;
    • Saviz, Proshat;
    • Nejad, Mohammad Zarei;
    • Tivay, Ali;
    • Shahriari, Hossein Ali;
    • Maleki, Alireza;
    • Ahmadi, Seyed Sajad;
    • Sargazi, Monireh;
    • Cremers, Frans P. M.;
    • Najafi, Maryam;
    • Vona, Barbara;
    • Haaf, Thomas;
    • Bahena-Carbajal, Paulina;
    • Moghadasi, Afrooz
    Publication type:
    Article
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    Tissue Extract from Brittle Star Undergoing Arm Regeneration Promotes Wound Healing in Rat.

    Published in:
    Marine Drugs, 2023, v. 21, n. 7, p. 381, doi. 10.3390/md21070381
    By:
    • Afshar, Alireza;
    • Khoradmehr, Arezoo;
    • Nowzari, Fariborz;
    • Baghban, Neda;
    • Zare, Masoud;
    • Najafi, Maryam;
    • Keshavarzi, Seyedeh Zahra;
    • Zendehboudi, Fatemeh;
    • Mohebbi, Gholamhossein;
    • Barmak, Alireza;
    • Mohajer, Fatemeh;
    • Basouli, Nahid;
    • Keshtkar, Mohammadreza;
    • Iraji, Aida;
    • Sari Aslani, Fatemeh;
    • Irajie, Cambyz;
    • Nabipour, Iraj;
    • Mahmudpour, Mehdi;
    • Tanideh, Nader;
    • Tamadon, Amin
    Publication type:
    Article
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    Expanding the clinical phenotype of IARS2-related mitochondrial disease.

    Published in:
    BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0709-3
    By:
    • Vona, Barbara;
    • Maroofian, Reza;
    • Bellacchio, Emanuele;
    • Najafi, Maryam;
    • Thompson, Kyle;
    • Alahmad, Ahmad;
    • He, Langping;
    • Ahangari, Najmeh;
    • Rad, Abolfazl;
    • Shahrokhzadeh, Sima;
    • Bahena, Paulina;
    • Mittag, Falk;
    • Traub, Frank;
    • Movaffagh, Jebrail;
    • Amiri, Nafise;
    • Doosti, Mohammad;
    • Boostani, Reza;
    • Shirzadeh, Ebrahim;
    • Haaf, Thomas;
    • Diodato, Daria
    Publication type:
    Article
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    Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function.

    Published in:
    Human Mutation, 2019, v. 40, n. 3, p. 267, doi. 10.1002/humu.23694
    By:
    • Rehman, Atteeq U.;
    • Najafi, Maryam;
    • Kambouris, Marios;
    • Al‐Gazali, Lihadh;
    • Makrythanasis, Periklis;
    • Rad, Abolfazl;
    • Maroofian, Reza;
    • Rajab, Anna;
    • Stark, Zornitza;
    • Hunter, Jill V.;
    • Bakey, Zeineb;
    • Tokita, Mari J.;
    • He, Weimin;
    • Vetrini, Francesco;
    • Petersen, Andrea;
    • Santoni, Federico A.;
    • Hamamy, Hanan;
    • Wu, Kaman;
    • Al‐Jasmi, Fatma;
    • Helmstädter, Martin
    Publication type:
    Article
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    Cover Image, Volume 40, Issue 3.

    Published in:
    Human Mutation, 2019, v. 40, n. 3, p. i, doi. 10.1002/humu.22892
    By:
    • Rehman, Atteeq U.;
    • Najafi, Maryam;
    • Kambouris, Marios;
    • Al‐Gazali, Lihadh;
    • Makrythanasis, Periklis;
    • Rad, Abolfazl;
    • Maroofian, Reza;
    • Rajab, Anna;
    • Stark, Zornitza;
    • Hunter, Jill V.;
    • Bakey, Zeineb;
    • Tokita, Mari J.;
    • He, Weimin;
    • Vetrini, Francesco;
    • Petersen, Andrea;
    • Santoni, Federico A.;
    • Hamamy, Hanan;
    • Wu, Kaman;
    • Al‐Jasmi, Fatma;
    • Helmstädter, Martin
    Publication type:
    Article
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