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[Related PubMed/MEDLINE]
Total Number of Papers: 16
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| Abbreviation |
: HSCR |
| Long Form |
: Hirschsprung |
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| No. |
Year |
Title |
Co-occurring Abbreviation |
| 1 |
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 |
| 2 |
2017 |
Multiple endocrine neoplasia 2B: Differential increase in enteric nerve subgroups in muscle and mucosa. |
MEN 2B |
| 3 |
2013 |
Potential use of skin-derived precursors (SKPs) in establishing a cell-based treatment model for Hirschsprung's disease. |
SKPs, SKPs |
| 4 |
2011 |
Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans. |
DLL3, ENCCs |
| 5 |
2010 |
HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Hirschsprung Disease. |
--- |
| 6 |
2006 |
Molecular mechanisms of RET-induced Hirschsprung pathogenesis. |
--- |
| 7 |
2006 |
Multiple endocrine neoplasia 2B presenting with pseudo-Hirschsprung's disease. |
MEN 2B, MTC |
| 8 |
2006 |
PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations. |
NB |
| 9 |
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 |
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