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Items: 27

1.

Novel DNA variation of GPR54 gene in familial central precocious puberty.

Ghaemi N, Ghahraman M, Noroozi Asl S, Vakili R, Fardi Golyan F, Moghbeli M, Abbaszadegan MR.

Ital J Pediatr. 2019 Jan 11;45(1):10. doi: 10.1186/s13052-019-0601-6.

2.

Mutational analysis of ARSB gene in mucopolysaccharidosis type VI: identification of three novel mutations in Iranian patients.

Malekpour N, Vakili R, Hamzehloie T.

Iran J Basic Med Sci. 2018 Sep;21(9):950-956. doi: 10.22038/IJBMS.2018.27742.6760.

3.
4.

Mutations in HNF1A Gene are not a Common Cause of Familial Young-Onset Diabetes in Iran.

Moghbeli M, Naghibzadeh B, Ghahraman M, Fatemi S, Taghavi M, Vakili R, Abbaszadegan MR.

Indian J Clin Biochem. 2018 Jan;33(1):91-95. doi: 10.1007/s12291-017-0648-3. Epub 2017 Apr 13.

5.

Novel mutations and their genotype-phenotype correlations in patients with Noonan syndrome, using next-generation sequencing.

Tafazoli A, Eshraghi P, Pantaleoni F, Vakili R, Moghaddassian M, Ghahraman M, Muto V, Paolacci S, Golyan FF, Abbaszadegan MR.

Adv Med Sci. 2018 Mar;63(1):87-93. doi: 10.1016/j.advms.2017.07.001. Epub 2017 Sep 26.

PMID:
28957739
6.

The Report of Three Rare Cases of the Niemann-pick Disease in Birjand, South Khorasan, Eastern Iran.

Noroozi Asl S, Vakili R, Ghaemi N, Eshraghi P.

Iran J Child Neurol. 2017 Summer;11(3):53-56.

7.

Iranian Gender-Nonconforming Children Will Not Benefit from the Omission of Gender Incongruence in Children Diagnosis.

Khorashad BS, Talaei A, Bordbar MRF, Modares-Gharavi M, Vakili R, Taghavi Razavizadeh R, Koohestani L, Afkhamizadeh M.

Arch Sex Behav. 2017 Nov;46(8):2509-2510. doi: 10.1007/s10508-016-0888-y. Epub 2016 Oct 27. No abstract available.

PMID:
27787638
8.

Acute Intermittent Porphyria: A Diagnostic Challenge.

Vakili R, Armanpoor P.

Iran J Pediatr. 2016 May 10;26(3):e5238. doi: 10.5812/ijp.5238. eCollection 2016 Jun. No abstract available.

9.

Identification of four novel mutations of the WFS1 gene in Iranian Wolfram syndrome pedigrees.

Ghahraman M, Abbaszadegan MR, Vakili R, Hosseini S, Fardi Golyan F, Ghaemi N, Forghanifard MM.

Acta Diabetol. 2016 Dec;53(6):899-904. doi: 10.1007/s00592-016-0884-7. Epub 2016 Jul 13.

PMID:
27412528
10.
11.

Comparison of Novel Coronary Artery Disease Risk Factors between Obese and Normal Adolescent.

Kouzehgaran S, Vakili R, Nematy M, Safarian M, Ghayour-Mobarhan M, Khajedaluee M.

Iran J Med Sci. 2015 Jul;40(4):322-7.

12.

Determination of Biological Variance and Validation of a Fluorometric Assay for Measurement of α-l-Iduronidase Activity in Dried Blood Spots Samples: The First Experience in Iran.

Abdi M, Hakhamaneshi MS, Alaei MR, Azadi NA, Vakili R, Zamanfar D, Taghikhani M, Khatami S.

Indian J Clin Biochem. 2015 Jul;30(3):318-22. doi: 10.1007/s12291-014-0444-2. Epub 2014 Jul 30.

13.

Comparison of body mass index in children of two different regions of welfare.

Shapouri Moghadam A, Safarian M, Vakili R, Ehteshamfar SM.

Acta Med Iran. 2015;53(2):122-4.

14.

Validation of Urinary Glycosaminoglycans in Iranian patients with Mucopolysaccharidase type I: The effect of urine sedimentation characteristics.

Abdi M, Hakhamaneshi MS, Alaei MR, Azadi NA, Vakili R, Zamanfar D, Taghikhani M, Khatami S.

Iran J Child Neurol. 2014 Fall;8(4):39-45.

15.

The Association between Carotid Intima-Media Thickness and the Duration of Type 1 Diabetes in Children.

Pezeshki Rad M, Farrokh D, Vakili R, Omidbakhsh M, Mohammadi M.

Iran J Pediatr. 2014 Jun;24(3):249-54.

16.

Hearing disorders in Turner's syndrome: a survey from Iran.

Bakhshaee M, Vakili R, Nourizadeh N, Rajati M, Ahrari A, Movahed R.

Eur Arch Otorhinolaryngol. 2015 Dec;272(12):3705-8. doi: 10.1007/s00405-014-3371-1. Epub 2014 Dec 23.

PMID:
25534285
17.

Teaching final-year medical students in a paediatric ambulatory care unit.

Behmanesh F, Ahanchian H, Vakili R, Ahanchian N, Bagheri S.

Clin Teach. 2014 Aug;11(5):361-4. doi: 10.1111/tct.12150.

PMID:
25041669
18.

Novel mutation in the SLC19A2 gene in an Iranian family with thiamine-responsive megaloblastic anemia: a series of three cases.

Ghaemi N, Ghahraman M, Abbaszadegan MR, Baradaran-Heravi A, Vakili R.

J Clin Res Pediatr Endocrinol. 2013 Sep 10;5(3):199-201. doi: 10.4274/Jcrpe.969.

19.

Two novel mutations in CYP11B1 and modeling the consequent alterations of the translated protein in classic congenital adrenal hyperplasia patients.

Abbaszadegan MR, Hassani S, Vakili R, Saberi MR, Baradaran-Heravi A, A'rabi A, Hashemipour M, Razzaghi-Azar M, Moaven O, Baratian A, Ahadian M, Keify F, Meurice N.

Endocrine. 2013 Aug;44(1):212-9. doi: 10.1007/s12020-012-9861-2. Epub 2013 Jan 24. Erratum in: Endocrine. 2013 Aug;44(1):271.

PMID:
23345044
20.

Investigation of the effect of high dairy diet on body mass index and body fat in overweight and obese children.

Ghayour-Mobarhan M, Sahebkar A, Vakili R, Safarian M, Nematy M, Lotfian E, Khorashadizadeh M, Tavallaie S, Dahri M, Ferns G.

Indian J Pediatr. 2009 Nov;76(11):1145-50. doi: 10.1007/s12098-009-0231-x.

PMID:
20012799
21.

Tumor induced hypercalcemia in a patient with mediastinal synovial sarcoma.

Vakili R, Hiradfar M, Zabolinejad N, Badiei Z.

J Pediatr Endocrinol Metab. 2007 Jul;20(7):841-5.

PMID:
17849748
22.

Three novel CYP21A2 mutations and their protein modelling in patients with classical 21-hydroxylase deficiency from northeastern Iran.

Baradaran-Heravi A, Vakili R, Robins T, Carlsson J, Ghaemi N, A'rabi A, Abbaszadegan MR.

Clin Endocrinol (Oxf). 2007 Sep;67(3):335-41. Epub 2007 Jun 15.

PMID:
17573904
23.

Nager's acrofacial dysostosis with hypertrophic cardiomyopathy.

Kahrom M, Abbaszadegan MR, Kahrom H, Vakili R.

Saudi Med J. 2006 Oct;27(10):1578-81.

PMID:
17013486
24.

Hypogonadotropic hypogonadism associated with cleidocranial dysostosis.

Vakili R, Jalali F.

J Pediatr Endocrinol Metab. 2005 Sep;18(9):917-9.

PMID:
16279370
25.

Molecular analysis of the CYP21 gene and prenatal diagnosis in families with 21-hydroxylase deficiency in northeastern Iran.

Vakili R, Baradaran-Heravi A, Barid-Fatehi B, Gholamin M, Ghaemi N, Abbaszadegan MR.

Horm Res. 2005;63(3):119-24. Epub 2005 Mar 17.

PMID:
15775714
26.

Precocious puberty: an unusual presentation of juvenile hypothyroidism.

Vakili R.

Ann Saudi Med. 2004 Mar-Apr;24(2):145-7. No abstract available.

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