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Items: 1 to 20 of 141

1.

A new variant of the acrorenal syndrome associated with bilateral oligomeganephronic hypoplasia.

Miltényi M, Balogh L, Schmidt K, Detre Z, Hernády T, Czeizel A.

Eur J Pediatr. 1984 Apr;142(1):40-3.

PMID:
6714259
2.

Acrorenal syndrome associated with visual defect.

al Salloum AA, al Rasheed SA, al Husain MA, al Mugeiren MM, al Rikabi AS, al Sohaibani MO.

Pediatr Nephrol. 1996 Dec;10(6):759-60.

PMID:
8971900
3.

Acrorenal syndrome in an adult--presentation with proteinuria, hypertension, and glomerular lesions.

Zeier M, Tariverdian G, Waldherr R, Andrassy K, Ritz E.

Am J Kidney Dis. 1989 Sep;14(3):221-4.

PMID:
2773925
4.

Autosomal recessive acrorenal syndrome.

Miltényi M, Czeizel AE, Balogh L, Detre Z.

Am J Med Genet. 1992 Jul 15;43(5):789-90.

PMID:
1344975
5.

Acrorenal syndrome: further observations.

Houlston R, MacDermot K.

Clin Dysmorphol. 1992 Jan;1(1):23-8. Review.

PMID:
1342854
6.

Acrorenal syndrome in a child with renal failure.

Akl K.

Am J Med Genet. 1994 Feb 15;49(4):447. No abstract available.

PMID:
8179725
7.

Oligomeganephronic renal hypoplasia.

Broyer M, Soto B, Gagnadoux MF, Adi M, Rica C, Gubler MC.

Adv Nephrol Necker Hosp. 1997;26:47-63. No abstract available.

PMID:
8922124
8.

Townes-Brocks syndrome presenting as end stage renal failure.

Newman WG, Brunet MD, Donnai D.

Clin Dysmorphol. 1997 Jan;6(1):57-60. No abstract available.

PMID:
9072124
9.

Oligomeganephronic renal hypoplasia.

Detre Z, Miltényi M.

Pathol Res Pract. 1984 Mar;178(4):416-9. No abstract available.

PMID:
6728725
10.

Oligohydramnios, cause of the nonrenal features of Potter's syndrome, including pulmonary hypoplasia.

Thomas IT, Smith DW.

J Pediatr. 1974 Jun;84(6):811-5. No abstract available.

PMID:
4826613
11.

[Case of oligomeganephronia in an 11-year-old boy].

Sieniawska M, Bialasik D, Helczyński L.

Pol Tyg Lek. 1976 Dec 20;31(51):2191-2. Polish. No abstract available.

PMID:
1005209
12.

Acro-renal-mandibular syndrome.

Halal F, Desgranges MF, Leduc B, Thêorét G, Bettez P.

Am J Med Genet. 1980;5(3):277-84.

PMID:
7405959
13.

Renal dysplasia/hypoplasia, Williams Syndrome phenotype and non-Hodgkin lymphoma in the same patient: only a coincidence?

Urisarri-Ruiz de Cortázar A, Calvo MG, Donsión MV, Iraola GA, Sánchez JM.

Pediatr Nephrol. 2009 May;24(5):1081-4. doi: 10.1007/s00467-008-1069-6. Epub 2008 Dec 9.

PMID:
19066974
14.

Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndrome.

Wieczorek D, Gillessen-Kaesbach G, Plewa S, Passarge E.

Clin Genet. 1996 Feb;49(2):98-102.

PMID:
8740922
15.

Twenty-one-year-old male with congenital anomalies, obstructive uropathy and chronic renal failure: is this a case of Townes Brocks syndrome?

Unuigbe EI, Azubike CA, Okaka EI, Osarenkhoe JO, Onuora VC.

Niger J Clin Pract. 2007 Mar;10(1):91-4.

PMID:
17668723
16.

Digito-reno-cerebral syndrome: confirmation of Eronen syndrome.

Le Merrer M, David A, Goutieres F, Briard ML.

Clin Genet. 1992 Oct;42(4):196-8.

PMID:
1424243
17.

Severe acro-renal-uterine-mandibular syndrome.

Evans JA, Phillips S, Reed M, Chodirker BN.

Am J Med Genet. 2000 Jul 3;93(1):67-73.

PMID:
10861684
18.

Renal defects and limb deficiencies in 197 infants: is it possible to define the "acrorenal syndrome"?

Kroes HY, Olney RS, Rosano A, Liu Y, Castilla EE, Cocchi G, De Vigan C, Martínez-Frías ML, Mastroiacovo P, Merlob P, Mutchinick O, Ritvanen A, Stoll C, van Essen AJ, Cobben JM, Cornel MC.

Am J Med Genet A. 2004 Aug 30;129A(2):149-55.

PMID:
15316969
20.

[Oligomeganephronia].

Detre Z, Tarján G, Külkey O, Balogh L, Schmidt K.

Morphol Igazsagugyi Orv Sz. 1984 Jan;24(1):53-9. Hungarian. No abstract available.

PMID:
6694651

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