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■ Abbreviation / Long Form : HSCR / Hirschsprung

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Total Number of Papers: 16
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Abbreviation:   HSCR  (>> Co-occurring Abbreviation)
Long Form:   Hirschsprung
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No. Year Title Co-occurring Abbreviation
2019 A Metagenomics Study on Hirschsprung's Disease Associated Enterocolitis: Biodiversity and Gut Microbial Homeostasis Depend on Resection Length and Patient's Clinical History. IRB, TCSA
2017 Multiple endocrine neoplasia 2B: Differential increase in enteric nerve subgroups in muscle and mucosa. MEN 2B
2013 Potential use of skin-derived precursors (SKPs) in establishing a cell-based treatment model for Hirschsprung's disease. SKPs, SKPs
2011 Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans. DLL3, ENCCs
2010 HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Hirschsprung Disease. ---
2006 Molecular mechanisms of RET-induced Hirschsprung pathogenesis. ---
2006 Multiple endocrine neoplasia 2B presenting with pseudo-Hirschsprung's disease. MEN 2B, MTC
2006 PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations. NB
2005 Transanal pull-through for Hirschsprung disease. ---
10  2003 PMX2B, a new candidate gene for Hirschsprung's disease. CGH, EDN
11  2001 [From gene to disease; from the RET gene to multiple endocrine neoplasia types 2A and 2B, sporadic and familial medullary thyroid carcinoma, Hirschsprung disease and papillary thyroid carcinoma]. FMTC, MEN2A, 2B
12  1998 Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. MR
13  1996 A mutation in the RET proto-oncogene in Hirschsprung's disease affects the tyrosine kinase activity associated with multiple endocrine neoplasia type 2A and 2B. MEN 2A, MEN 2B
14  1995 Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) rat. EDN3, EDNRB, sl
15  1995 Loss of function effect of RET mutations causing Hirschsprung disease. ---
16  1993 Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung disease. MEN 2A