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Items: 1 to 20 of 303

1.

Ivemark syndrome: asplenia with kidney collecting duct cysts and polysplenia with cerebellar cyst.

Krźelj V, Kragić I, Glavina-Durdov M, Jakl R, Bucat M, Kuzmić-Prusac I.

Turk J Pediatr. 2000 Jul-Sep;42(3):234-8.

PMID:
11105625
2.

Defects in laterality with emphasis on heterotaxy syndromes with asplenia and polysplenia: an autopsy case series at a single institution.

Burton EC, Olson M, Rooper L.

Pediatr Dev Pathol. 2014 Jul-Aug;17(4):250-64. doi: 10.2350/13-11-1406-OA.1.

PMID:
24735181
3.

Ivemark syndrome with agenesis of the corpus callosum: a case report with a review of the literature.

Noack F, Sayk F, Ressel A, Berg C, Gembruch U, Reusche E.

Prenat Diagn. 2002 Nov;22(11):1011-5. Review.

PMID:
12424766
4.

Polysplenia with left ventricular hypoplasia and partial anomalous pulmonary venous connection.

Salazar J, Martinez F, Valero MI, Frias EC.

Acta Cardiol. 1976;31(6):483-90.

PMID:
1088053
5.

Familial asplenia, other malformations, and sudden death.

Katcher AL.

Pediatrics. 1980 Mar;65(3):633-5.

PMID:
7360556
6.
7.

Ivemark syndrome in association with congenital septum transversum defect and pancreatic divisum.

Sharma S, Gangopadhyay AN, Sharma SP.

Indian J Gastroenterol. 2006 Mar-Apr;25(2):94-6.

PMID:
16763342
8.

Aortic outflow obstruction in visceral heterotaxy: a study based on twenty postmortem cases.

Van Praagh S, Geva T, Friedberg DZ, Oechler H, Colli A, Frigiola A, Van Praagh R.

Am Heart J. 1997 May;133(5):558-69.

PMID:
9141378
9.

Asplenia and polysplenia syndrome.

Shinohara Y, Komiya S, Nakashima A, Nakashima T, Takeuchi S, Ono E, Yukizane S, Tanaka C, Matsuishi T, Koga T, Hieda Y, Nakashima H, Ichikawa A.

Acta Pathol Jpn. 1982 May;32(3):505-11.

PMID:
7102311
10.

Abnormal P wave axis in congenital heart disease associated with asplenia and polysplenia.

Momma K, Linde LM.

J Electrocardiol. 1969 Oct;2(4):395-402. No abstract available.

PMID:
5382237
11.

Biliary atresia with associated structural malformations in Canadian infants.

Guttman OR, Roberts EA, Schreiber RA, Barker CC, Ng VL; Canadian Pediatric Hepatology Research Group..

Liver Int. 2011 Nov;31(10):1485-93. doi: 10.1111/j.1478-3231.2011.02578.x.

PMID:
21819536
12.

Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.

Leonardi ML, Pai GS, Wilkes B, Lebel RR.

Am J Med Genet. 2001 Aug 15;102(3):237-42. Review.

PMID:
11484200
14.

["Ivemark syndrome": severe congenital cyanogenic heart disease, complex thoraco-abdominal heterotaxia and asplenia or polysplenia].

Neimann N, Pernot C, Gentin G, Vert P, Worms AM.

Pediatrie. 1966 Jul-Aug;21(5):511-32. French. No abstract available.

PMID:
5943512
15.

Atrial isomerism in the heterotaxy syndromes with asplenia, or polysplenia, or normally formed spleen: an erroneous concept.

Van Praagh R, Van Praagh S.

Am J Cardiol. 1990 Dec 15;66(20):1504-6. No abstract available.

PMID:
2252000
16.

Interrupted inferior vena cava in asplenia syndrome and a review of the hereditary patterns of visceral situs abnormalities.

Ruscazio M, Van Praagh S, Marrass AR, Catani G, Iliceto S, Van Praagh R.

Am J Cardiol. 1998 Jan 1;81(1):111-6. Review.

PMID:
9462624
17.

[The "Ivemark syndrome" severe cyanogenic congenital cardiopathy, complex thoraco-abdominal heterotaxia and asplenia or polysplenia].

Neimann N, Pernot C, Vert P, Worms AM.

Arch Mal Coeur Vaiss. 1966 Jun;59(6):876-900. French. No abstract available.

PMID:
4960659
18.

Prenatal diagnosis of asplenia/polysplenia syndrome.

Chitayat D, Lao A, Wilson RD, Fagerstrom C, Hayden M.

Am J Obstet Gynecol. 1988 May;158(5):1085-7.

PMID:
3369489
19.

The modified Fontan operation for asplenia and polysplenia syndromes.

Humes RA, Feldt RH, Porter CJ, Julsrud PR, Puga FJ, Danielson GK.

J Thorac Cardiovasc Surg. 1988 Aug;96(2):212-8.

PMID:
3398543
20.

Polysplenia syndrome with common atrioventricular canal and persistent truncus arteriosus.

Arai H, Harada K, Tamura M, Okamura T, Takada G.

Tohoku J Exp Med. 1995 Oct;177(2):171-7.

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