X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
arteriohepatic dysplasia (206) 206
index medicus (179) 179
humans (178) 178
alagille syndrome (115) 115
male (93) 93
female (88) 88
pediatrics (63) 63
child (61) 61
infant (59) 59
child, preschool (54) 54
alagille syndrome - genetics (50) 50
paucity (48) 48
alagille syndrome - complications (47) 47
genetics & heredity (47) 47
cholestasis (43) 43
children (39) 39
gastroenterology & hepatology (37) 37
serrate-jagged proteins (37) 37
interlobular bile-ducts (36) 36
adult (33) 33
jagged-1 protein (33) 33
adolescent (32) 32
alagille syndrome - diagnosis (32) 32
mutations (31) 31
disease (30) 30
infant, newborn (28) 28
mutation (27) 27
alagille syndrome - pathology (26) 26
deletion (26) 26
liver (26) 26
transplantation (25) 25
calcium-binding proteins (24) 24
intercellular signaling peptides and proteins (24) 24
alagille-syndrome (23) 23
bile-ducts (23) 23
jagged1 gene (23) 23
liver transplantation (23) 23
alagille syndrome - surgery (22) 22
liver - pathology (22) 22
liver-transplantation (21) 21
biliary atresia (19) 19
frequency (19) 19
phenotype (19) 19
proteins - genetics (19) 19
abridged index medicus (18) 18
diagnosis (18) 18
membrane proteins (18) 18
membrane proteins - genetics (18) 18
expression (17) 17
jagged1 (17) 17
retrospective studies (17) 17
gene (16) 16
nutrition & dietetics (16) 16
pedigree (16) 16
surgery (16) 16
syndrome arteriohepatic dysplasia (16) 16
facies (14) 14
family (14) 14
features (14) 14
follow-up studies (14) 14
human jagged1 (14) 14
ophthalmology (14) 14
calcium-binding proteins - genetics (13) 13
hepatocellular-carcinoma (13) 13
intercellular signaling peptides and proteins - genetics (13) 13
malformations (13) 13
prognosis (13) 13
urology & nephrology (13) 13
alagille syndrome - physiopathology (12) 12
alagille's syndrome (12) 12
childhood (12) 12
syndrome (12) 12
20p (11) 11
alagille syndrome - diagnostic imaging (11) 11
animals (11) 11
bile ducts, intrahepatic - abnormalities (11) 11
chromosomes, human, pair 20 (11) 11
diagnosis, differential (11) 11
intrahepatic cholestasis (11) 11
liver diseases (11) 11
medicine & public health (11) 11
morbidity (11) 11
pathology (11) 11
abnormalities, multiple - genetics (10) 10
magnetic resonance imaging (10) 10
vascular anomalies (10) 10
alagille syndrome - metabolism (9) 9
anomalies (9) 9
genetic aspects (9) 9
hypertension (9) 9
radiology, nuclear medicine & medical imaging (9) 9
abnormalities (8) 8
cholestasis - etiology (8) 8
chromosome 20 (8) 8
chromosome deletion (8) 8
chromosome-20 (8) 8
defects (8) 8
dna mutational analysis (8) 8
genotype (8) 8
heart defects, congenital - genetics (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Case Report - Alagille syndrome with prominent skin manifestations, 12/2005
Alagille syndrome, a rare genetic disorder with autosomal dominant transmission, manifests 5 major features: paucity of interlobular bile ducts, characteristic... 
Alagille syndrome, Arteriohepatic dysplasia, Xanthomata
Journal
Zdorovʹe Rebenka, ISSN 2224-0551, 03/2015, Volume 10, Issue 2.1.62.1, pp. 128 - 132
The article presents a clinical case of a child with a rare nosology — Alagille syndrome. Among the causes of neonatal cholestasis, Alagille syndrome is ranked... 
Alagille syndrome | children | arteriohepatic dysplasia
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2006, Volume 79, Issue 1, pp. 169 - 173
Journal Article
Gastroenterology, ISSN 0016-5085, 03/2018, Volume 154, Issue 4, pp. 1080 - 1095
Alagille syndrome is a genetic disorder characterized by cholestasis, ocular abnormalities, characteristic facial features, heart defects, and vertebral... 
Heart | Vertebrae | Jagged1 | Liver | Notch | Development | Alagille | Kidney | STEM-CELLS | HEPATOCYTES | PROTEIN | REGENERATION | ARTERIOHEPATIC DYSPLASIA | BILE-DUCT DEVELOPMENT | MICE | DIFFERENTIATION | GASTROENTEROLOGY & HEPATOLOGY | NOTCH2 MUTATIONS | Index Medicus | Abridged Index Medicus
Journal Article
Indian Pediatrics, ISSN 0019-6061, 2014, Volume 51, Issue 4, pp. 314 - 316
Background: Alagille Syndrome is a rare genetic disease characterized by abnormalities of the intrahepatic biliary ducts with cholestasis along with... 
Posterior embryotoxon | Arteriohepatic dysplasia | Mutation | PEDIATRICS
Journal Article
Paediatrica Indonesiana, ISSN 0030-9311, 02/2017, Volume 41, Issue 1, pp. 47 - 55
Alagille syndrome (AGS) Is a common form of familial intrahepatic choleslasis, an autosomal dominant disorder due to defects in Jagged1 gene. It Is... 
liver disease | Alagille syndrome | cholestasis | prognosis | arteriohepatic dysplasia
Journal Article
Pediatric and Developmental Pathology, ISSN 1093-5266, 11/2018, Volume 21, Issue 6, pp. 585 - 589
Alagille syndrome is associated with decreased bile ducts, cardiac abnormalities, vertebral body fusion defects, and a typical facies. While regenerative... 
hepatic adenoma | magnetic resonance imaging | pathology | gadoxetate disodium | liver | arteriohepatic dysplasia | Alagille | pediatric | HEPATOCELLULAR ADENOMA | CLASSIFICATION | PEDIATRICS | CARCINOMA | Liver Neoplasms - etiology | Adenoma - diagnosis | Liver Neoplasms - diagnosis | Humans | Alagille Syndrome - complications | Adenoma - etiology | Male | Child | Index Medicus
Journal Article
JOURNAL OF HYPERTENSION, ISSN 0263-6352, 07/2012, Volume 30, Issue 7, pp. 1300 - 1306
Alagille syndrome is a rare congenital multisystem disorder that may involve heart disease and pulmonary or peripheral artery stenosis. We report the clinical... 
renal artery obstruction | JAGGED1 GENE | Alagille syndrome | ARTERIOHEPATIC DYSPLASIA | renovascular | BILE-DUCTS | midaortic syndrome | CHILDREN | FAMILY | VASCULAR ANOMALIES | RENOVASCULAR HYPERTENSION | HYPOPLASIA | PERIPHERAL VASCULAR DISEASE | MUTATIONS | ABDOMINAL COARCTATION | hypertension
Journal Article
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, ISSN 1936-2625, 2017, Volume 10, Issue 4, pp. 4913 - 4917
Alagille syndrome (ALGS) is a multisystem autosomal dominant disorder caused by defects in the Notch signaling pathway. The classical criteria for ALGS... 
DIAGNOSIS | JAGGED1 GENE | Alagille syndrome | INTRAHEPATIC CHOLESTASIS | PAUCITY | ARTERIOHEPATIC DYSPLASIA | JAG1 gene | CLINICAL-FEATURES | PATHOLOGY | BILE-DUCTS | liver failure | gene variations | ONCOLOGY | atypical | FREQUENCY | MUTATIONS
Journal Article
Journal Article