Results 81 to 90 of about 5,957 (204)

Función esplénica en la anemia drepanocítica Splenic function in sickle cell anemia

Revista Cubana de Hematología, Inmunología y Hemoterapia, 2004
Se realizó gammagrafía esplénica con Tc 99m sulfuro coloidal y Tc 99m metildifosfonato a 30 niños con anemia drepanocítica en condiciones basales. Se formaron 3 grupos: el primero incluyó niños entre 0 y 5 años, el segundo entre 6 y 10 y el tercero entre
Ileana Nordet Carrera, Aramís Núñez Quintana, Andrea Menéndez Veitía, Sergio Machín García, Tania García Peralta, Leonel Torres la Roche, Juan Batista Cuéllar, Maura Wade Mateo, Alejandro González Otero, Eva Svarch   +9 more
doaj  

Congenital Asplenia in Mice and Humans with Mutations in a Pbx/Nkx2-5/p15 Module

, 2012
SummaryThe molecular determinants of spleen organogenesis and the etiology of isolated congenital asplenia (ICA), a life-threatening human condition, are unknown. We previously reported that Pbx1 deficiency causes organ growth defects including asplenia.
Lenti, Elisa, Mahlaoui, Nizar, Prall, Owen W.J., Selleri, Licia, Koss, Matthew, Brendolan, Andrea, Elliott, David A., Bojilova, Ekaterina, Solloway, Mark, Hidaka, Chisa, Bolze, Alexandre, Harvey, Richard P., Saggese, Matilde, Casanova, Jean-Laurent, Capellini, Terence D., Chang, Ching-Pin, Boisson, Bertrand   +16 more
core   +1 more source

The genetic dissection of isolated congenital asplenia in humans

, 2014
This is my PhD thesis done in the laboratory of Human Genetics of Infectious Diseases at the Rockefeller University, under the supervision of Dr. Jean-Laurent Casanova.
Alexandre Bolze (675624)
core   +1 more source

PENTALOGY OF CANTRELL WITH COMPLETE ECTOPIA CORDIS IN A FETUS WITH ASPLENIA

, 2012
Cantrell's Pentalogy (CP) is a rare, mainly sporadic spectrum of congenital midline thoracoabdominal defects including sternal anomalies, ventral diaphragmatic hernia, partial absence of the pericardium, supraumbilical abdominal wall defects and ...
Ludwig K, Salmaso R, Manara R, Margiotti K, RUGGE, MASSIMO, COSMI, ERICH, Iaria L, De Luca A, Citton V   +8 more
core   +1 more source

ePoster

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Asplenia: O Risco Esquecido na Síndrome de Heterotaxia

, 2014
A síndrome de heterotaxia, frequentemente denominada como isomerismo, designa um grupo de patologias em que a habitual disposição dos orgãos torácicos e abdominais está alterada.
Martins, Maymone, Ferreira, Rosário, Anjos, Rui   +2 more
core   +1 more source

A CASE OF COR BILOCULARE ACCOMPANIED BY POLYSPLENIA [PDF]

Acta Medica Iranica, 1972
The clinical history and necroscopic fi ndings of a 3 -} year old girl - involved in cor biloculare was reported. In th is case dextrotransposition of the great a rteries and polysplenia was observed. The majority of cor biloculare cases appearing in the
M. S. ROJHAN
doaj   +2 more sources

Congenital Asplenia In A Surgical Patient

, 2008
Congenital asplenia is rare and could occur sporadically or less commonly as part of a syndrome. Sporadic or isolated congenital asphenia is not usually associated with significant morbidity.
Okpala, N C, N C Okpala, Petit, S H, S H Petit   +3 more
core   +1 more source

Esophageal Varices in Congenital Heart Disease with Total Anomalous Pulmonary Venous Connection

, 2009
Total anomalous pulmonary venous connection (TAPVC) is an uncommon congenital anomaly in which the anatomical presentations vary widely among patients.
李瑤華;吳美環;陳世杰, LI, YIU-WAH;WU, MEI-HWAN;CHEN, SHYH- JYE   +1 more
core  

Clinical implications of dextrocardia based on four visceroatrial situs studies

Pediatrics and Neonatology
Background: Previous studies on congenital heart diseases (CHD) associated with dextrocardia were based on selective patient databases and did not reflect the full spectrum of dextrocardia in the general population.
Mao-Sheng Hwang, Ching-Chia Kuo, Chao-Jan Wang, Wen-Jen Su, Jaw-Ji Chu, Hung-Tao Chung, Hsiang-Ju Hsiao, Yi-Jung Chang   +7 more
doaj   +1 more source