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Items: 7

1.

Epidemiology of isolated preaxial polydactyly type I: data from the Polish Registry of Congenital Malformations (PRCM).

Materna-Kiryluk A, Jamsheer A, Wisniewska K, Wieckowska B, Limon J, Borszewska-Kornacka M, Sawulicka-Oleszczuk H, Szwalkiewicz-Warowicka E, Latos-Bielenska A.

BMC Pediatr. 2013 Feb 19;13:26. doi: 10.1186/1471-2431-13-26.

2.

Maternal reproductive history and the risk of isolated congenital malformations.

Materna-Kiryluk A, Więckowska B, Wiśniewska K, Borszewska-Kornacka MK, Godula-Stuglik U, Limon J, Rusin J, Sawulicka-Oleszczuk H, Szwałkiewicz-Warowicka E, Walczak M; Members of PRCM Working Group.

Paediatr Perinat Epidemiol. 2011 Mar;25(2):135-43. doi: 10.1111/j.1365-3016.2010.01186.x. Epub 2011 Jan 12.

PMID:
21281326
3.

Paternally inherited proinsulin mutations may result in earlier onset of monogenic diabetes mutation identity effect in monogenic diabetes.

Fendler W, Borowiec M, Antosik K, Jaroszewska-Swiatek B, Szwalkiewicz-Warowicka E, Malecki M, Mysliwiec M, Mlynarski W.

Diabetes Care. 2011 Jan;34(1):e9. doi: 10.2337/dc10-1142. No abstract available.

PMID:
21193618
4.

Parental age as a risk factor for isolated congenital malformations in a Polish population.

Materna-Kiryluk A, Wiśniewska K, Badura-Stronka M, Mejnartowicz J, Wieckowska B, Balcar-Boroń A, Czerwionka-Szaflarska M, Gajewska E, Godula-Stuglik U, Krawczyński M, Limon J, Rusin J, Sawulicka-Oleszczuk H, Szwalkiewicz-Warowicka E, Walczak M, Latos-Bieleńska A.

Paediatr Perinat Epidemiol. 2009 Jan;23(1):29-40. doi: 10.1111/j.1365-3016.2008.00979.x.

PMID:
19228312
5.

Comparative study of clinical characteristics of amniotic rupture sequence with and without body wall defect: further evidence for separation.

Jamsheer A, Materna-Kiryluk A, Badura-Stronka M, Wiśniewska K, Wieckowska B, Mejnartowicz J, Balcar-Boroń A, Borszewska-Kornacka M, Czerwionka-Szaflarska M, Gajewska E, Godula-Stuglik U, Krawczynski M, Limon J, Rusin J, Sawulicka-Oleszczuk H, Szwałkiewicz-Warowicka E, Swietliński J, Walczak M, Latos-Bieleńska A.

Birth Defects Res A Clin Mol Teratol. 2009 Mar;85(3):211-5. doi: 10.1002/bdra.20555.

PMID:
19180633
6.

[Syndrome of congenital malformations and dysmorphic features in a newborn with partial trisomy 16q due to maternal translocation t(9;16)(p24;q13)].

Luberda-Zapaśnik J, Midro AT, Szwałkiewicz-Warowicka E.

Pediatr Pol. 1995 Sep;70(9):769-73. Polish.

PMID:
8657511
7.

[Chronology of ultrasonographic course of neonatal intraventricular hemorrhage stage III].

Monset-Couchard M, Szwalkiewicz-Warowicka E, de Bethmann O.

Pediatrie. 1993;48(1):69-75. French.

PMID:
8392696
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