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Abbreviation: HSCR
Appearance Frequency: 658 time(s)
Long forms: 11

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
Hirschsprung disease
(628 times)
Pediatrics
(182 times)
ENS (77 times)
GDNF (35 times)
SNPs (33 times)
1993 A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10.
Hirschsprung
(16 times)
Genetics, Medical
(6 times)
MEN 2B (3 times)
MEN 2A (2 times)
SKPs (2 times)
1993 Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung disease.
hematopoietic stem cell rescue
(4 times)
Neoplasms
(4 times)
EFS (2 times)
OS (2 times)
TT (2 times)
1994 The role of autologous hematopoietic stem cell transplantation in hematologic malignancy.
Homelessness Screening Clinical Reminder
(3 times)
Internal Medicine
(1 time)
VHA (2 times)
EMR (1 time)
SSVF (1 time)
2019 Predictive modeling of housing instability and homelessness in the Veterans Health Administration.
hematologic stem cell reinfusion
(1 time)
Hematology
(1 time)
BuMel (1 time)
VHR (1 time)
2018 Feasibility of Busulfan Melphalan and Stem Cell Rescue After 131I-MIBG and Topotecan Therapy for Refractory or Relapsed Metastatic Neuroblastoma: The French Experience.
Hirschsprung′s disease
(1 time)
Pediatrics
(1 time)
--- 2018 [Syndromic Hirschsprung′s disease and its mode of inheritance].
Hirschsprung's disease patients
(1 time)
General Surgery
(1 time)
ARDRA (1 time)
HAEC (1 time)
2010 Genomics approach to the analysis of bacterial communities dynamics in Hirschsprung's disease-associated enterocolitis: a pilot study.
HSCR and/or ARM
(1 time)
Molecular Biology
(1 time)
ARMs (1 time)
Hh (1 time)
OR (1 time)
2016 Hedgehog gene polymorphisms are associated with the risk of Hirschsprung's disease and anorectal malformation in a Chinese population.
human congenital disorder, Hirschsprung disease
(1 time)
Genetics
(1 time)
Edn3 (1 time)
ls (1 time)
1995 A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease.
10  hypotonia, short segment Hirschsprung disease
(1 time)
Genetics, Medical
(1 time)
--- 1999 A Hirschsprung disease locus at 22q11?
11  isolated-Hirschsprung disease
(1 time)
Medicine
(1 time)
CNVs (1 time)
2013 Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia.