Results 81 to 90 of about 4,848,621 (165)

Generative AI as a support tool for the histopathological diagnosis of Hirschsprung disease

openBackground: La diagnosi di malattia di Hirschsprung (HD) viene confermata attraverso l'analisi istopatologica delle biopsie rettali. Tuttavia, l'esame manuale dei vetrini istologici è un processo laborioso e soggetto ad errori, il che evidenzia la ...
SEGAT, FRANCESCA
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A Hirschsprung disease locus at 22q11?

, 1999
We report a boy with truncus arteriosus, dysmorphic features, developmental delay, passing hypotonia, short segment Hirschsprung disease (HSCR), and paroxysmal hypoventilation.
Meijers, JHC, Kerstjens-Frederikse, WS, van Essen, AJ, Hofstra, RMW, Buys, CHCM   +4 more
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Acute Intussusception Following a Pull-Through Operation for Hirschsprung Disease

, 2008
Acute post-operative intussusception is a rare. This is a report of two cases of acute intestinal intussusception were observed in two children aged 14 months and 2.5 years following operation for Hirschsprung\'s disease.
Nandiolo, R, Vody, L, Bankole, S R, Mobiot, M, Mouafo, T F, Coulibaly, D   +5 more
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Colorectal cancer at the anastomotic site following childhood surgery for hirschsprung disease: a rare case report

World Journal of Surgical Oncology
Background The present case of a colorectal adenocarcinoma at the anastomotic site of a colorectal anastomosis after childhood surgery for Hirschsprung disease is a rare report of such pathology.
Matthias Mehdorn, Philipp Rhode, Jan-Hendrik Gosemann, Katja Grunwald, Hans-Jonas Meyer, Martin Lacher, Sigmar Stelzner   +6 more
doaj   +1 more source

Hirschsprung Disease: development & treatment avenues [PDF]

, 2019
The work of this thesis investigates the development of, and treatment options for, Hirschsprung disease (HSCR). We explore the missing heritability that is seen in HSCR, modes of development and differentiation of the progenitors of the ENS ...
MacKenzie, K.C. (Katherine)
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Management of comorbid congenital diaphragmatic hernia and Hirschsprung disease: A case report

Journal of Pediatric Surgery Case Reports
Introduction: Congenital diaphragmatic hernia (CDH) and Hirschsprung disease (HD) are each rare, potentially life-threatening congenital diseases. Early recognition of combined presentation allows for optimal management.
Nzuekoh N. Nchinda, Carrie Foster, Jimiane Ashe, Matthew B. Dellinger, Samuel E. Rice-Townsend   +4 more
doaj   +1 more source

Evaluation and Management of Total Colonic Hirschsprung Disease: A Comprehensive Review From the American Pediatric Surgical Association (APSA) Hirschsprung Disease Interest Group.

BACKGROUND: Children with total colonic Hirschsprung disease (TCHD) are a unique group of patients with pre- and postoperative management challenges. This review provides a rational, expert-based approach to diagnosing and managing TCHD.
Rialon, Kristy L, Segura, Bradley, Wood, Richard J, Frischer, Jason S, Rollins, Michael D, Lim, Irene Isabel P, Levitt, Marc A, Bokova, Elizaveta, Gosain, Ankush, American Pediatric Surgical Association Hirschsprung Disease Interest Group, Rentea, Rebecca M, Langer, Jacob C, Nandivada, Prathima   +12 more
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Frequency of RET mutations in long- and short-segment Hirschsprung disease.

, 1997
Hirschsprung disease, or congenital aganglionic megacolon, is a genetic disorder of neural crest development affecting 1:5,000 newborns. Mutations in the RET proto-oncogene, repeatedly identified in the heterozygous state in both long- and short-segment ...
CELLI, J., Yin, L, Casasa, J M, Cass, D T, Abramowicz, Marc, Bocciardi, R, BARONE, V., Yamaguchi, S., Bachmann, C., LARSSON, L. T., PASINI, B., Romeo, G, Matthieu, J.M., ABRAMOWICZ, M. J., KRISTOFFERSSON, U., Martucciello, G, BARIC, I., Little, M., CECCHERINI, I., SILENGO, M., CASASA, J. M., Kravcenkiene, I, Baric, I, MARTUCCIELLO, G., Lerone, M, Silengo, M, BOCCIARDI, R., Orii, T., ROMEO, G., LERONE, M., Hashimoto, T., Fukao, T., Barone, V, Larsson, L T, Vanderwinden, Jean-Marie, VANDERWINDEN, J. M., Bolino, A, Kristoffersson, U, BOLINO, A., Pasini, B, KRAVCENKIENE, I., Song, X.Q., Seri, M, SERI, M., YIN, L., Wells, C., Ceccherini, I, Kondo, N., Celli, I, Ceccherini I, Pasini B, Larsson LT, Kristoffersson U, Lindblom, A,, Casasa JM, Barone V, Celli I, Silengo M, BorresenDale, AL, Lerone M, Cass DT, Kravcenkiene I, Abramowicz MJ, Romeo G, Martucciello G, Bocciardi R, Bolino A, Baric I, Seri M, Vanderwinden JM, ZeladaHedman, M, Yin L   +71 more
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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
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Genetics of gastrointestinal disease: dismotility disorders, intestinal polyposis and gene therapy [PDF]

, 2008
Auricchio, Renata
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