Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Gideon Hirschfield
NOTCH2mutations in Alagille Syndrome
Journal of Medical Genetics
Genetics
Related publications
Alagille Syndrome: Family Studies.
Journal of Medical Genetics
Genetics
ALAGILLE SYNDROME AS a CHALLENGING CLINICAL CASE IN PEDIATRIC PRACTICE (Case Report)
Inter Collegas
A New Model of Alagille Syndrome With Broad Phenotypic Representation
Gastroenterology
Hepatology
Gastroenterology
Extracranial and Intracranial Vasculopathy With “Moyamoya Phenomenon” in Association With Alagille Syndrome
Frontiers in Neurology
Neurology
Novel Heterozygous Mutations in JAG1 and NOTCH2 Genes in a Neonatal Patient With Alagille Syndrome
Case Reports in Pediatrics
Critical Region in 2q31.2q32.3 Deletion Syndrome: Report of Two Phenotypically Distinct Patients, One With an Additional Deletion in Alagille Syndrome Region
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
An Autosomal Recessive Form of Alagille-Like Syndrome That Is Not Linked to JAG1
Genetics in Medicine
Medicine
Genetics
SR-BI- And ABCA1-mediated Cholesterol Efflux to Serum From Patients With Alagille Syndrome
Journal of Lipid Research
Biochemistry
Endocrinology
Cell Biology
DoUble Resin Casting Micro Computed Tomography (DUCT) Reveals Biliary and Vascular Pathology in a Mouse Model of Alagille Syndrome
