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Recurrent synovitis of hip and MEFV gene related arthritis in children.

• Authors : Salehzadeh F; Pediatric Rheumatology, Pediatric Department, Bouali Children's Hospital, Ardabil University of Medical Sciences (ARUMS), Ardabil, Iran.; Mirzarahimi M

Subjects: Arthritis, Juvenile*/Arthritis, Juvenile*/Arthritis, Juvenile*/blood ; Arthritis, Juvenile*/Arthritis, Juvenile*/Arthritis, Juvenile*/diagnosis ; Arthritis, Juvenile*/Arthritis, Juvenile*/Arthritis, Juvenile*/genetics

• Source: Pediatric rheumatology online journal [Pediatr Rheumatol Online J] 2020 Aug 10; Vol. 18 (1), pp. 63. Date of Electronic Publication: 2020 Aug 10.Publisher: BioMed Central Country of Publication: England NLM ID: 101248897 Publication Model: Electronic Cited Medium:

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"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes.

• Source: Molecular Cytogenetics (17558166). 2012, Vol. 5 Issue 1, p9-13. 5p. 2 Charts.

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New insight into clinical heterogeneity and inheritance diversity of FBLN5-related cutis laxa.

• Authors : Gharesouran, Jalal; Hosseinzadeh, Hassan; Ghafouri-Fard, Soudeh

Subjects: SKIN; VENTRICULAR septal defects; TWINSIRAN

• Source: Orphanet Journal of Rare Diseases; 1/28/2021, Vol. 16 Issue 1, p1-13, 13p

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Familial resemblance and family-based heritability of nutrients intake in Iranian population: Tehran cardiometabolic genetic study.

• Authors : Teymoori F; Department of Nutrition, School of Public Health, Iran University of Medical Sciences, Tehran, Iran.; Akbarzadeh M

Subjects: Pantothenic Acid* ; Cardiovascular Diseases*; Female

• Source: BMC public health [BMC Public Health] 2023 Sep 14; Vol. 23 (1), pp. 1789. Date of Electronic Publication: 2023 Sep 14.Publisher: BioMed Central Country of Publication: England NLM ID: 100968562 Publication Model: Electronic Cited Medium:

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Dilated cardiomyopathy caused by a pathogenic nucleotide variant in RBM20 in an Iranian family.

• Authors : Malakootian M; Cardiogenetics Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.; Bagheri Moghaddam M

Subjects: Cardiomyopathy, Dilated*/Cardiomyopathy, Dilated*/Cardiomyopathy, Dilated*/genetics; Adult ; Heterozygote

• Source: BMC medical genomics [BMC Med Genomics] 2022 May 08; Vol. 15 (1), pp. 106. Date of Electronic Publication: 2022 May 08.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium:

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Epidemiology of familial multiple sclerosis in Iran: a national registry-based study.

• Authors : Salehi Z; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.; Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Sina Hospital, Hassan Abad Square, Tehran, Iran.

Subjects: Multiple Sclerosis*/Multiple Sclerosis*/Multiple Sclerosis*/epidemiology; Cross-Sectional Studies ; Female

• Source: BMC neurology [BMC Neurol] 2022 Mar 05; Vol. 22 (1), pp. 76. Date of Electronic Publication: 2022 Mar 05.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium:

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