نتائج البحث

Comprehensive copy number analysis of spinal muscular atrophy among the Iranian population.

• Authors : Khanbazi A; Kariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran.; Genetics Research Center, University of Social Welfare & Rehabilitation Sciences, Tehran, Iran.

Subjects: Muscular Atrophy, Spinal*/Muscular Atrophy, Spinal*/Muscular Atrophy, Spinal*/genetics ; Muscular Atrophy, Spinal*/Muscular Atrophy, Spinal*/Muscular Atrophy, Spinal*/epidemiology ; Survival of Motor Neuron 1 Protein*/Survival of Motor Neuron 1 Protein*/Survival of Motor Neuron 1 Protein*/genetics

• Source: Scientific reports [Sci Rep] 2024 Dec 02; Vol. 14 (1), pp. 29880. Date of Electronic Publication: 2024 Dec 02.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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A Rare Case of Hypoplasia of the Paranasal Sinuses and Atrophy of All Three Turbinates.

• Authors : Alizadeh, N.¹ ; Paryab, S.²; Hamze, A. Shah³

• Source: Journal of Babol University of Medical Sciences. 2021, Vol. 23 Issue 1, p105-108. 4p.

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The effect of oxytocin vaginal gel on vaginal atrophy in postmenopausal women: a randomized controlled trial.

• Authors : Zohrabi I; Menopause Andropause Research Center, Midwifery Department, Nursing & Midwifery School, Ahvaz Jundishapur University of Medical Sciences, Golestan Ave, Ahvaz, Iran.; Abedi P

Subjects: Atrophy/Atrophy/Atrophy/*drug therapy ; Oxytocin/Oxytocin/Oxytocin/*administration & dosage ; Postmenopause/Postmenopause/Postmenopause/*drug effects

• Source: BMC women's health [BMC Womens Health] 2020 May 19; Vol. 20 (1), pp. 108. Date of Electronic Publication: 2020 May 19.Publisher: BioMed Central Country of Publication: England NLM ID: 101088690 Publication Model: Electronic Cited Medium: Internet ISSN: 1472-6874

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Homozygous Mutation in TWNK Cases Ataxia, Sensorineural Hearing Loss and Optic Nerve Atrophy.

• Authors : Jamali F; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Ghaedi H

Subjects: DNA Helicases* ; Mitochondrial Proteins*; Spinocerebellar Degenerations/Spinocerebellar Degenerations/Spinocerebellar Degenerations/*geneticsInfantile onset spinocerebellar ataxia

• Source: Archives of Iranian medicine [Arch Iran Med] 2019 Dec 01; Vol. 22 (12), pp. 728-730. Date of Electronic Publication: 2019 Dec 01.Publisher: Academy of Medical Sciences of I.R. Iran Country of Publication: Iran NLM ID: 100889644

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A comprehensive overview of SMN and NAIP copy numbers in Iranian SMA patients.

• Authors : Savad S; Genome-Nilou Laboratory, Tehran, Iran. .; Ashrafi MR

Subjects: DNA Copy Number Variations* ; Muscular Atrophy, Spinal*/Muscular Atrophy, Spinal*/Muscular Atrophy, Spinal*/genetics; Humans

• Source: Scientific reports [Sci Rep] 2023 Feb 24; Vol. 13 (1), pp. 3202. Date of Electronic Publication: 2023 Feb 24.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Finite Element Assessment of a Novel Patient‐Specific Mandibular Implant for Severely Atrophic Ridge.

• Authors : Parhiz, Alireza; Nourishirazi, Reza; Asadi, Amirali

Subjects: MANDIBLE surgery; DENTAL implants; BONE resorptionIRAN

• Source: BioMed Research International; 8/29/2024, Vol. 2024, p1-7, 7p

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The sign of unilateral neck semispinalis capitis muscle atrophy in patients with chronic non-specific neck pain.

• Authors : Rezasoltani, Asghar¹; Ahmadipoor, Alireza¹; Khademi-Kalantari, Khosro¹

• Source: Journal of Back & Musculoskeletal Rehabilitation. 2012, Vol. 25 Issue 1, p67-72. 6p.

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Incidental findings in brain CT scans of patients with head trauma.

• Authors : Alinezhad, Marzieh; Alikhani, Fariba; Bamarinejad, Fatemeh

Subjects: CROSS-sectional method; CONSENSUS (Social sciences); PATIENTSIRAN

• Source: Frontiers in Emergency Medicine; Spring2024, Vol. 8 Issue 2, p1-6, 6p

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A novel variant in ASNS gene responsible for syndromic intellectual disability and microcephaly: Case report and literature review.

• Authors : Jahanpanah M; Department of Genetics and Pathology, Ardabil University of Medical Sciences, Ardabil, Iran.; Mokhtari D

Subjects: Microcephaly*/Microcephaly*/Microcephaly*/genetics ; Microcephaly*/Microcephaly*/Microcephaly*/diagnosis ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/genetics

• Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Apr; Vol. 12 (4), pp. e2424.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print Cited Medium: Internet ISSN:

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Pelvic hydatid cyst with uncommon sciatalgia manifestation: a case report.

• Authors : Maddah, Ghodratolah¹; Shabahang, Hossein¹ ; Noghabi, Reza Sharifi²

• Source: Tehran University Medical Journal. Nov2013, Vol. 71 Issue 8, p541-545. 5p.

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