Results 101 to 110 of about 9,792 (217)

Peritoneal mucinous carcinomatosis in a patient with a history of Hirschsprung's disease: The role of home parenteral nutrition Carcinomatosis mucinosa peritoneal en un paciente con antecedente de enfermedad de Hirschsprung: El papel de la nutrición parenteral

Nutrición Hospitalaria, 2007
A case of peritoneal mucinous carcinomatosis in a patient who suffered a Hirschsprung disease 30 year before is presented. TH present condition caused an irreversible intestinal obstruction and the patients received home parenteral nutrition without ...
J. M. Moreno-Villares, A. Mañas-Rueda, M. León-Sanz   +2 more
doaj  

Hirschsprung’s Disease [PDF]

Archives of Disease in Childhood, 1964
openaire   +2 more sources

Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination

Revista Chilena de Radiología, 2012
El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1.
David Ibáñez M, Ana Vela M, Beatriz Izquierdo H, Carolina Muel G   +3 more
doaj  

Appendix tip biopsy for Total colonic aganglionosis: technical aspects and diagnostic accuracy in a prospective cohort of 107 pediatric patients. [PDF]

Pediatr Surg Int
Lindert J, Stigler L, Sternke-Curvello C, Erbersdobler A, Märzheuser S.   +4 more
europepmc   +1 more source

Hirschsprung's disease [PDF]

Postgraduate Medical Journal, 1967
openaire   +2 more sources

Gastrointestinal symptoms and association to food items in children with hirschsprung disease: a multinational patient-reported outcome study from Latin America and Spain. [PDF]

Pediatr Surg Int
Scaramella C, Telborn L, Davidson J, Day H, de Andres Crespo M, Busoni V, Lobos P, Lindert J.   +7 more
europepmc   +1 more source

CYP4F22-Related Autosomal Recessive Congenital Ichthyosis Associated With Hirschsprung Disease and Bartter-Like Renal Manifestations. [PDF]

J Med Cases
Alqahtani JM.
europepmc   +1 more source

Corrigendum to “Mesenchymal Stem Cells Attenuates Hirschsprung diseases-Associated Enterocolitis by Reducing M1 Macrophages Infiltration via COX-2 Dependent Mechanism” [J Pediatr Surg 59 (2024) 1498–1514]

Journal of Pediatric Surgery Open
Xinyao Meng, Jun Xiao, Jing Wang, Minxian Sun, Xuyong Chen, Luyao Wu, Ke Chen, Zejian Li, ChenZhao Feng, Didi Zhuansun, Jixin Yang, Xiaojuan Wu, Donghai Yu, Wei Li, Yonghua Niu, Ying He, Mingfa Wei, Feng Chen, Bo Xiong, Jiexiong Feng, Tianqi Zhu   +20 more
doaj   +1 more source

DOENÇA DE HIRSCHSPRUNG: ASPECTOS NUTRICIONAIS

, 2019
127DOENÇA DE HIRSCHSPRUNG: ASPECTOS NUTRICIONAISMariah Oliveira A. de Figueredo*Érika Aparecida de Azevedo Pereira**RESUMOAs duas fases da Doença de Hirschsprung(DH)–pré e pós-operatória –podem apresentar condições clínicas como: constipação intestinal ...
de Figueredo, Mariah Oliveira A., Pereira, Érika Aparecida de Azevedo   +1 more
core  

Hirschsprung\u27s Disease Prevalence in Europe: A Register Based Study

Background: Hirschsprung\u27s disease is a congenital gut motility disorder, characterised by the absence of the enteric ganglion cells along the distal gut.
Sipek, Antonin, Wellesley, Diana, Addor, Marie-Claude, Calzolari, Elisa, Doray, Berenice, Rissmann, Anke, Rankin, Judith, Randrianaivo, Hanitra, Kooshnood, Babak, Dias, Carlos Matias, McDonnell, Bob, Balku, Eszter, Curran, Rhonda, Nelen, Vera, Tucker, David, O\u27Mahony, Mary, Garne, Ester, Gatt, Miriam, Thompson, Rosie, Bianchi, Fabrizio, Klugsoyr, Kari, Rounding, Catherine, Van Kammen-Bergman, Jerieke, Barisic, Ingeborg, Queisser-Luft, Annette, Haeusler, Martin, Matos, Carmen, Materna-Kiryluk, Anna, Mullaney, Carmel, Best, Kate E., Draper, Elizabeth, Zymak-Zakutnia, Natalyna, Arriola, Larraitz   +32 more
core   +1 more source