Publications by authors named "Ali Talea"

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Comprehensive Iranian guidelines for the diagnosis and management of mitochondrial disorders: an evidence- and consensus-based approach.
Setila Dalili, Noushin Rostampour, Seyedeh Tahereh Mousavi, Saeid Sadeghi Joni, Nejat Mahdieh, Ali Talea

Orphanet J Rare Dis· December 2025

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A Report of Dual Presentations of Pseudo-TORCH Syndrome 1 and MCC2 Deficiency and Review of the Literature.
Ali Talea, Shiva Bayat, Golazin Shahbodagh Khan, Neda Pak, Solmaz Aziz-Ahari

Mol Syndromol· August 2025

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Expanding the Clinical Phenotype Associated with the Gene; Report of a Patient with Short Stature, Microcephaly and Hearing Loss.
Shima Zamanian Najafabadi, Zeinab Ghorbanoghli, Zhila Ghaderi, Fariba Afroozan, Ali Talea

Arch Iran Med· May 2025

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Safety and effectiveness of a biosimilar somatropin (Cinnatropin®) in children and adolescents receiving growth hormone therapy over 1 year: a registry-based phase IV study.
Ali Rabbani, Maryam Razzaghy-Azar, Zohreh Karamizadeh, Mahin Hashemipour, Rahim Vakili, Ali Talea

Eur J Pediatr· March 2025

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Comprehensive Iranian guidelines for the diagnosis and management of maple syrup urine disease: an evidence- and consensus- based approach.
Noushin Rostampour, Setila Dalili, Hossein Moravej, Zhila Afshar, Negar Yazdani, Ali Talea

Orphanet J Rare Dis· January 2025

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Meglitinide (repaglinide) therapy in permanent neonatal diabetes mellitus: two case reports.
Maryam Razzaghy-Azar, Mitra Nourbakhsh, Ali Talea, Mahsa Mohammad Amoli, Mona Nourbakhsh

J Med Case Rep· October 2021

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Identification of a novel nonsense mutation and a missense substitution in the AGPAT2 gene causing congenital generalized lipodystrophy type 1.
Amirreza Haghighi, Maryam Razzaghy-Azar, Ali Talea, Mahnaz Sadeghian, Sian Ellard

Eur J Med Genet· November 2012

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