156 related articles for article (PubMed ID: 26557043)
1. Asplenia in children with congenital heart disease as a cause of poor outcome.
Erdem SB; Genel F; Erdur B; Ozbek E; Gulez N; Mese T
Cent Eur J Immunol; 2015; 40(2):266-9. PubMed ID: 26557043
[TBL] [Abstract][Full Text] [Related]
2. Asplenia as a cause of sudden unexpected death in childhood.
Kanthan R; Moyana T; Nyssen J
Am J Forensic Med Pathol; 1999 Mar; 20(1):57-9. PubMed ID: 10208339
[TBL] [Abstract][Full Text] [Related]
3. Sporadic isolated congenital asplenia with fulminant pneumococcal meningitis: a case report and updated literature review.
Iijima S
BMC Infect Dis; 2017 Dec; 17(1):777. PubMed ID: 29254492
[TBL] [Abstract][Full Text] [Related]
4. Familial asplenia, other malformations, and sudden death.
Katcher AL
Pediatrics; 1980 Mar; 65(3):633-5. PubMed ID: 7360556
[TBL] [Abstract][Full Text] [Related]
5. Familial isolated congenital asplenia: a rare, frequently hereditary dominant condition, often detected too late as a cause of overwhelming pneumococcal sepsis. Report of a new case and review of 31 others.
Gilbert B; Menetrey C; Belin V; Brosset P; de Lumley L; Fisher A
Eur J Pediatr; 2002 Jul; 161(7):368-72. PubMed ID: 12111187
[TBL] [Abstract][Full Text] [Related]
6. The absent and vanishing spleen: congenital asplenia and hyposplenism--two case reports.
Halbertsma FJ; Neeleman C; Weemaes CM; van Deuren M
Acta Paediatr; 2005 Mar; 94(3):369-71. PubMed ID: 16028659
[TBL] [Abstract][Full Text] [Related]
7. [Isolated congenital asplenia--a rare cause of severe pneumococcal sepsis].
Shachor-Meyouhas Y; Sprecher H; Kassis I
Harefuah; 2010 Aug; 149(8):486-9, 552. PubMed ID: 21341424
[TBL] [Abstract][Full Text] [Related]
8. Congenital asplenia study: clinical and laboratory characterisation of adults with congenital asplenia.
Butel-Simoes GI; Jones P; Wood EM; Spelman D; Woolley IJ; Ojaimi S
Ann Hematol; 2022 Jul; 101(7):1421-1434. PubMed ID: 35451619
[TBL] [Abstract][Full Text] [Related]
9. Case report of congenital asplenia presenting with Haemophilus influenzae type a (Hia) sepsis: an emerging pediatric infection in Minnesota.
Albrecht T; Poss K; Issaranggoon Na Ayuthaya S; Triden L; Schleiss KL; Schleiss MR
BMC Infect Dis; 2019 Nov; 19(1):947. PubMed ID: 31703560
[TBL] [Abstract][Full Text] [Related]
10. [Congenital asplenia and pneumococcal purpura fulminans in a pediatric patient: case report with pathological findings and review].
Bertrán S K; Donoso F A; Cruces R P; Díaz R F; Arriagada S D
Rev Chilena Infectol; 2009 Feb; 26(1):55-9. PubMed ID: 19350161
[TBL] [Abstract][Full Text] [Related]
11. 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; 17(4):250-64. PubMed ID: 24735181
[TBL] [Abstract][Full Text] [Related]
12. Invasive pneumococcal infections in children with asplenia.
Schutze GE; Mason EO; Barson WJ; Kim KS; Wald ER; Givner LB; Tan TQ; Bradley JS; Yogev R; Kaplan SL
Pediatr Infect Dis J; 2002 Apr; 21(4):278-82. PubMed ID: 12075756
[TBL] [Abstract][Full Text] [Related]
13. Intestinal obstruction in asplenia syndrome: report of three cases.
Tu ST; Wu JM; Yeh BH; Ke WL; Lin JH; Tzeng CC
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994; 35(1):70-7. PubMed ID: 8178646
[TBL] [Abstract][Full Text] [Related]
14. Asplenia syndrome: insight into embryology through an analysis of cardiac and extracardiac anomalies.
Phoon CK; Neill CA
Am J Cardiol; 1994 Mar; 73(8):581-7. PubMed ID: 8147305
[TBL] [Abstract][Full Text] [Related]
15. Isolated Congenital Asplenia in an Asymptomatic Patient: A Very Rare Diagnosis.
Dinis-Ferreira S; Lemos C; Caldeira M; Homem-Costa M; da Luz Brazão M; Aveiro F
Eur J Case Rep Intern Med; 2020; 7(4):001429. PubMed ID: 32309250
[TBL] [Abstract][Full Text] [Related]
16. Extracardiac anomalies in prenatally diagnosed heterotaxy syndrome.
Gottschalk I; Stressig R; Ritgen J; Herberg U; Breuer J; Vorndamme A; Strizek B; Willruth A; Geipel A; Gembruch U; Berg C
Ultrasound Obstet Gynecol; 2016 Apr; 47(4):443-9. PubMed ID: 25847110
[TBL] [Abstract][Full Text] [Related]
17. Germline 3p22.1 microdeletion encompassing RPSA gene is an ultra-rare cause of isolated asplenia.
Oszer A; Bąbol-Pokora K; Kołtan S; Pastorczak A; Młynarski W
Mol Cytogenet; 2021 Nov; 14(1):51. PubMed ID: 34781974
[TBL] [Abstract][Full Text] [Related]
18. Congenital asplenia and anomalies of the gastrointestinal tract.
Mishalany H; Mahnovski V; Woolley M
Surgery; 1982 Jan; 91(1):38-41. PubMed ID: 7054905
[TBL] [Abstract][Full Text] [Related]
19. Sepsis and congenital asplenia.
Waldman JD; Rosenthal A; Smith AL; Shurin S; Nadas AS
J Pediatr; 1977 Apr; 90(4):555-9. PubMed ID: 320299
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
