Méhes K - Search Results

1

Family investigations in idiopathic hypercalciuria.

Harangi F, Méhes K. Harangi F, et al. Among authors: mehes k. Eur J Pediatr. 1993 Jan;152(1):64-8. doi: 10.1007/BF02072519. Eur J Pediatr. 1993. PMID: 8444209

2

Epithelial Ca(2+) channel (ECAC1) in autosomal dominant idiopathic hypercalciuria.

Müller D, Hoenderop JG, Vennekens R, Eggert P, Harangi F, Méhes K, Garcia-Nieto V, Claverie-Martin F, Os CH, Nilius B, J M Bindels R. Müller D, et al. Among authors: mehes k. Nephrol Dial Transplant. 2002 Sep;17(9):1614-20. doi: 10.1093/ndt/17.9.1614. Nephrol Dial Transplant. 2002. PMID: 12198212

3

Increased prevalence of minor anomalies in childhood malignancy.

Méhes K, Signer E, Plüss HJ, Müller HJ, Stalder G. Méhes K, et al. Eur J Pediatr. 1985 Sep;144(3):243-54. doi: 10.1007/BF00451951. Eur J Pediatr. 1985. PMID: 4054163

4

Minor morphological aberrations in children with isolated urinary tract malformations.

Méhes K, Pintér A. Méhes K, et al. Eur J Pediatr. 1990 Mar;149(6):399-402. doi: 10.1007/BF02009658. Eur J Pediatr. 1990. PMID: 2332007

5

Autosomal dominant inheritance of hypercalciuria.

Méhes K, Szelid Z. Méhes K, et al. Eur J Pediatr. 1980 May;133(3):239-42. doi: 10.1007/BF00496083. Eur J Pediatr. 1980. PMID: 7389737

6

Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia.

Morava E, Kárteszi J, Weisenbach J, Caliebe A, Mundlos S, Méhes K. Morava E, et al. Among authors: mehes k. Eur J Pediatr. 2002 Nov;161(11):619-22. doi: 10.1007/s00431-002-0977-x. Epub 2002 Oct 9. Eur J Pediatr. 2002. PMID: 12424590

7

Familial association of supernumerary nipple with renal cancer.

Mehes K. Mehes K. Cancer Genet Cytogenet. 1996 Feb;86(2):129-30. doi: 10.1016/0165-4608(95)00185-9. Cancer Genet Cytogenet. 1996. PMID: 8603338

8

Excess of malignancies in grandparents of children with malformations? Short communication.

Hadzsiev K, Tárnok A, Kosztolányi G, Méhes K. Hadzsiev K, et al. Among authors: mehes k. Acta Biol Hung. 2006 Mar;57(1):137-40. doi: 10.1556/ABiol.57.2006.1.14. Acta Biol Hung. 2006. PMID: 16646533

9

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency.

Komlósi K, Magyari L, Talián GC, Nemes E, Káposzta R, Mogyorósy G, Méhes K, Melegh B. Komlósi K, et al. Among authors: mehes k. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S15-9. doi: 10.1007/s10545-009-0926-1. Epub 2009 Feb 24. J Inherit Metab Dis. 2009. PMID: 19238580

10

Familial benign copper deficiency: an old case re-examined.

Méhes K, Petrovicz E. Méhes K, et al. Acta Paediatr Hung. 1988-1989;29(3-4):313-5. Acta Paediatr Hung. 1988. PMID: 2978614

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