The contribution of associated congenital anomalies in understanding Hirschsprung's disease.
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c-Ret-mediated hearing loss in mice with Hirschsprung diseaseNovel mechanisms of early upper and lower urinary tract patterning regulated by RetY1015 docking tyrosine in miceOrganotypic specificity of key RET adaptor-docking sites in the pathogenesis of neurocristopathies and renal malformations in mice.Novel association of severe neonatal encephalopathy and Hirschsprung disease in a male with a duplication at the Xq28 region.Hirschsprung's Disease and Associated Congenital Heart Defects: A Prospective Observational Study from a Single Institution.Complex pathogenesis of Hirschsprung's disease in a patient with hydrocephalus, vesico-ureteral reflux and a balanced translocation t(3;17)(p12;q11).A prospective observational study of associated anomalies in Hirschsprung's disease.A novel corrective pullthrough surgery in a mouse model of Hirschsprung's diseaseHirschsprung's disease associated with alopecia universalis congenita: a case report.Treatment and Patient Reported Outcome in Children with Hirschsprung Disease and Concomitant Congenital Heart Disease.Hirschsprung's disease and the brain.c-Ret-mediated hearing losses.Hearing impairments caused by genetic and environmental factors.Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.Advances in Hirschsprung disease genetics and treatment strategies: an update for the primary care pediatrician.Congenital anomalies of the kidney and urinary tract (CAKUT) associated with Hirschsprung's disease: a systematic review.Prevalence of Hirschsprung's disease in premature infants: a systematic review.Total colonic aganglionosis and Hirschsprung's disease: a review.Syndromic Hirschsprung's disease and associated congenital heart disease: a systematic review.Extraskeletal osteosarcoma of the orbit: A clinicopathologic case report and review of literature.Genetic Background of Hirschsprung Disease: A Bridge Between Basic Science and Clinical Application.The many faces of RET dysfunction in kidney.Mowat-Wilson syndrome: the first report of an association with central nervous system tumors.Hirschsprung's disease prevalence in Europe: a register based study.
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P2860
The contribution of associated congenital anomalies in understanding Hirschsprung's disease.
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2006 nî lūn-bûn
@nan
2006 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
The contribution of associated ...... anding Hirschsprung's disease.
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The contribution of associated ...... anding Hirschsprung's disease.
@en
The contribution of associated ...... anding Hirschsprung's disease.
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type
label
The contribution of associated ...... anding Hirschsprung's disease.
@ast
The contribution of associated ...... anding Hirschsprung's disease.
@en
The contribution of associated ...... anding Hirschsprung's disease.
@nl
prefLabel
The contribution of associated ...... anding Hirschsprung's disease.
@ast
The contribution of associated ...... anding Hirschsprung's disease.
@en
The contribution of associated ...... anding Hirschsprung's disease.
@nl
P2860
P1476
The contribution of associated ...... anding Hirschsprung's disease.
@en
P2093
P2860
P2888
P304
P356
10.1007/S00383-006-1655-2
P577
2006-03-04T00:00:00Z
P6179
1019707062