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Alport syndrome and other collagen disorders
Michelle N. Rheault
Pediatric Nephrology
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Chapter in Book/Report/Conference proceeding
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Keyphrases
Alport Syndrome
100%
COL4A1
100%
Collagen Disease
100%
Type IV Collagen
83%
Non-progressive
33%
COL4A6
33%
COL4A5
33%
Collagen Genes
33%
Clinical Manifestations
16%
Kidney Disease
16%
Heparan Sulfate Proteoglycans
16%
Laminin
16%
Basement Membrane
16%
Nephropathy
16%
Aneurysm
16%
Muscle Cramps
16%
Clinical Treatment
16%
Heterozygous mutation
16%
Sudden Sensorineural Hearing Loss (SSNHL)
16%
Pathological Diagnosis
16%
Clinical Pathology
16%
Collagen Type 1
16%
Thin Basement Membrane Nephropathy
16%
Microscopic Hematuria
16%
Inherited Kidney Disease
16%
Eye Abnormalities
16%
Glomerular Disorders
16%
Nidogen-1
16%
α-Chain
16%
Angiopathy
16%
Leiomyomatosis
16%
Medicine and Dentistry
Disease
100%
Alport Syndrome
100%
Collagen Type 4
100%
Nephropathy
80%
Basement Membrane
40%
Entactin
40%
Aneurysm
20%
Muscle Cramp
20%
Sensorineural Hearing Loss
20%
Collagen Type 1
20%
Proteoheparan Sulfate
20%
Clinical Genetics
20%
Eye Malformation
20%
Glomerular Disorder
20%
Vascular Disease
20%
Leiomyomatosis
20%
Alpha Chain
20%
Hematuria
20%
Laminin
20%
Biochemistry, Genetics and Molecular Biology
Type IV Collagen
100%
COL4A4
40%
COL4A5
40%
COL4A6
40%
Basement Membrane
40%
Entactin
40%
Genetics
20%
Alpha Chain
20%
Laminin
20%
Proteoglycan
20%
Heparan Sulfate
20%