Sallai A - Search Results

1

National registry of patients with juvenile idiopathic inflammatory myopathies in Hungary--clinical characteristics and disease course of 44 patients with juvenile dermatomyositis.

Constantin T, Ponyi A, Orbán I, Molnár K, Dérfalvi B, Dicso F, Kálovics T, Müller J, Garami M, Sallai A, Balogh Z, Szalai Z, Fekete G, Dankó K. Constantin T, et al. Among authors: sallai a. Autoimmunity. 2006 May;39(3):223-32. doi: 10.1080/08916930600622819. Autoimmunity. 2006. PMID: 16769656 Free article.

2

[Disease course, frequency of relapses and survival of patients with juvenile or adult dermatomyositis].

Constantin T, Ponyi A, Kálovics T, Orbán I, Molnár K, Dérfalvy B, Dicso F, Sallai A, Garami M, Balogh Z, Szalai Z, Fekete G, Dankó K. Constantin T, et al. Among authors: sallai a. Orv Hetil. 2007 Oct 21;148(42):1989-97. doi: 10.1556/OH.2007.27907. Orv Hetil. 2007. PMID: 17932005 Hungarian.

3

Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated cases.

Sallai A, Hosszú E, Gergics P, Rácz K, Fekete G. Sallai A, et al. Eur J Pediatr. 2008 Apr;167(4):441-6. doi: 10.1007/s00431-007-0532-x. Epub 2007 Jun 19. Eur J Pediatr. 2008. PMID: 17576593

4

Y-chromosome markers in Turner syndrome: Screening of 130 patients.

Sallai A, Sólyom J, Dobos M, Szabó J, Halász Z, Ságodi L, Niederland T, Kozári A, Bertalan R, Ugocsai P, Fekete G. Sallai A, et al. J Endocrinol Invest. 2010 Apr;33(4):222-7. doi: 10.1007/BF03345783. Epub 2009 Jul 21. J Endocrinol Invest. 2010. PMID: 19625757

5

Mutational analysis of Hungarian patients with androgen insensitivity syndrome.

Scheiber D, Barta C, Halász Z, Sallai A, Rácz K, Ságodi L, Fekete G, Hiort O, Sólyom J. Scheiber D, et al. Among authors: sallai a. J Pediatr Endocrinol Metab. 2003 Mar;16(3):367-73. doi: 10.1515/jpem.2003.16.3.367. J Pediatr Endocrinol Metab. 2003. PMID: 12705360

6

High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency.

Halász Z, Toke J, Patócs A, Bertalan R, Tömböl Z, Sallai A, Hosszú E, Muzsnai A, Kovács L, Sólyom J, Fekete G, Rácz K. Halász Z, et al. Among authors: sallai a. Endocrine. 2006 Dec;30(3):255-60. doi: 10.1007/s12020-006-0002-7. Endocrine. 2006. PMID: 17526936

7

[Examination of sex chromosome abnormalities in childhood].

Pinti É, Lengyel A, Sallai Á, Fekete G, Haltrich I. Pinti É, et al. Among authors: sallai a. Orv Hetil. 2018 Jul;159(27):1121-1128. doi: 10.1556/650.2018.31081. Orv Hetil. 2018. PMID: 29961370 Hungarian.

8

[Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome].

Ács OD, Péterfia B, Hollósi P, Haltrich I, Sallai Á, Luczay A, Buiting K, Horsthemke B, Török D, Szabó A, Fekete G. Ács OD, et al. Among authors: sallai a. Orv Hetil. 2018 Jan;159(2):64-69. doi: 10.1556/650.2018.30918. Orv Hetil. 2018. PMID: 29307221 Hungarian.

9

[The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study].

Dávid A, Butz H, Halász Z, Török D, Nyirő G, Muzsnai Á, Csákváry V, Luczay A, Sallai Á, Hosszú É, Felszeghy E, Tar A, Szántó Z, Fekete GL, Kun I, Patócs A, Bertalan R. Dávid A, et al. Among authors: sallai a. Orv Hetil. 2017 Aug;158(34):1351-1356. doi: 10.1556/650.2017.30829. Orv Hetil. 2017. PMID: 28823207 Hungarian.

10

Effect of diet and physical exercise treatment on insulin resistance syndrome of schoolchildren.

Szamosi A, Czinner A, Szamosi T, Sallai A, Hatunic M, Berla Z, Tomsits E, Almássy Z, Nolan JJ. Szamosi A, et al. Among authors: sallai a. J Am Coll Nutr. 2008 Feb;27(1):177-83. doi: 10.1080/07315724.2008.10719689. J Am Coll Nutr. 2008. PMID: 18460496

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