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Subcategories
This category has the following 4 subcategories, out of 4 total.
Pages in category "Metabolic disorders"
The following 200 pages are in this category, out of 300 total.
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- Aceruloplasminemia
- Adenylosuccinate lyase deficiency
- Adrenoleukodystrophy (patient information)
- Adult treatment panel guidelines (ATP III) for hypercholestrolemia
- ALA dehydratase deficiency
- Alcohol flush reaction
- Alkaptonuria
- Alkaptonuria (patient information)
- Alpha 1-antitrypsin deficiency (patient information)
- Amyloid purpura
- Amyloidosis (patient information)
C
- Confusion (patient information)
- Congenital disorder of glycosylation
- Congenital hyperinsulinism
- Congenital hyperinsulinism (patient information)
- Congenital hyperinsulinism case study one
- Congenital hyperinsulinism causes
- Congenital hyperinsulinism classification
- Congenital hyperinsulinism cost-effectiveness of therapy
- Congenital hyperinsulinism CT
- Congenital hyperinsulinism differential diagnosis
- Congenital hyperinsulinism epidemiology and demographics
- Congenital hyperinsulinism future or investigational therapies
- Congenital hyperinsulinism historical perspective
- Congenital hyperinsulinism history and symptoms
- Congenital hyperinsulinism laboratory findings
- Congenital hyperinsulinism medical therapy
- Congenital hyperinsulinism MRI
- Congenital hyperinsulinism natural history, complications and prognosis
- Congenital hyperinsulinism other diagnostic studies
- Congenital hyperinsulinism other imaging findings
- Congenital hyperinsulinism overview
- Congenital hyperinsulinism pathophysiology
- Congenital hyperinsulinism physical examination
- Congenital hyperinsulinism primary prevention
- Congenital hyperinsulinism risk factors
- Congenital hyperinsulinism screening
- Congenital hyperinsulinism secondary prevention
- Congenital hyperinsulinism surgery
- Congenital hyperinsulinism ultrasound
- Congenital hyperinsulinism x ray
- Crigler-Najjar syndrome (patient information)
D
- Dehydration
- Dehydration (patient information)
- Dehydration case study one
- Dehydration causes
- Dehydration classification
- Dehydration cost-effectiveness of therapy
- Dehydration differential diagnosis
- Dehydration electrocardiogram
- Dehydration epidemiology and demographics
- Dehydration future or investigational therapies
- Dehydration historical perspective
- Dehydration history and symptoms
- Dehydration laboratory findings
- Dehydration medical therapy
- Dehydration MRI
- Dehydration natural history, complications and prognosis
- Dehydration other diagnostic studies
- Dehydration other imaging findings
- Dehydration overview
- Dehydration pathophysiology
- Dehydration physical examination
- Dehydration primary prevention
- Dehydration risk factors
- Delayed milestone
- Disaccharidase
- Disorders of calcium metabolism
- Disorders of purine metabolism
G
- Galactose-1-phosphate uridylyltransferase galactosemia
- Galactosemia differential diagnosis
- Gilbert's syndrome
- Gilbert's syndrome (patient information)
- Gilbert's syndrome case study one
- Gilbert's syndrome causes
- Gilbert's syndrome cost-effectiveness of therapy
- Gilbert's syndrome differential diagnosis
- Gilbert's syndrome echocardiography or ultrasound
- Gilbert's syndrome epidemiology and demographics
- Gilbert's syndrome future or investigational therapies
- Gilbert's syndrome historical perspective
- Gilbert's syndrome history and symptoms
- Gilbert's syndrome laboratory findings
- Gilbert's syndrome medical therapy
- Gilbert's syndrome natural history, complications and prognosis
- Gilbert's syndrome other diagnostic studies
- Gilbert's syndrome other imaging findings
- Gilbert's syndrome overview
- Gilbert's syndrome pathophysiology
- Gilbert's syndrome physical examination
- Gilbert's syndrome prevention
- Glucoglycinuria
- Glycogen storage disease
- Glycogen storage disease type 0
- Glycogen storage disease type I
- Glycogen storage disease type I (patient information)
- Glycogen storage disease type I case study one
- Glycogen storage disease type I causes
- Glycogen storage disease type I classification
- Glycogen storage disease type I CT
- Glycogen storage disease type I diagnostic study of choice
- Glycogen storage disease type I differential diagnosis
- Glycogen storage disease type I electrocardiogram
- Glycogen storage disease type I epidemiology and demographics
- Glycogen storage disease type I historical perspective
- Glycogen storage disease type I history and symptoms
- Glycogen storage disease type I laboratory findings
- Glycogen storage disease type I medical therapy
- Glycogen storage disease type I MRI
- Glycogen storage disease type I natural history, complications and prognosis
- Glycogen storage disease type I other diagnostic studies
- Glycogen storage disease type I other imaging findings
- Glycogen storage disease type I overview
- Glycogen storage disease type I pathophysiology
- Glycogen storage disease type I physical examination
- Glycogen storage disease type I primary prevention
- Glycogen storage disease type I risk factors
- Glycogen storage disease type I screening
- Glycogen storage disease type I secondary prevention
- Glycogen storage disease type I surgery
- Glycogen storage disease type I ultrasound
- Glycogen storage disease type I x ray
- Glycogen storage disease type II
- Glycogen storage disease type II (patient information)
- Glycogen storage disease type II causes
- Glycogen storage disease type II classification
- Glycogen storage disease type II CT
- Glycogen storage disease type II diagnostic study of choice
- Glycogen storage disease type II differential diagnosis
- Glycogen storage disease type II echocardiography or ultrasound
- Glycogen storage disease type II electrocardiogram
- Glycogen storage disease type II epidemiology and demographics
- Glycogen storage disease type II historical perspective
- Glycogen storage disease type II history and symptoms
- Glycogen storage disease type II laboratory findings
- Glycogen storage disease type II medical therapy
- Glycogen storage disease type II MRI
- Glycogen storage disease type II natural history, complications and prognosis
- Glycogen storage disease type II other diagnostic studies
- Glycogen storage disease type II other imaging findings
- Glycogen storage disease type II overview
- Glycogen storage disease type II pathophysiology
- Glycogen storage disease type II physical examination
- Glycogen storage disease type II primary prevention
- Glycogen storage disease type II risk factors
- Glycogen storage disease type II screening
- Glycogen storage disease type II secondary prevention
- Glycogen storage disease type II surgery
- Glycogen storage disease type II x ray
- Glycogen storage disease type III
- Glycogen storage disease type III (patient information)
- Glycogen storage disease type III causes
- Glycogen storage disease type III classification
- Glycogen storage disease type III CT scan
- Glycogen storage disease type III diagnostic study of choice
- Glycogen storage disease type III differential diagnosis
- Glycogen storage disease type III echocardiography and ultrasound
- Glycogen storage disease type III electrocardiogram
- Glycogen storage disease type III epidemiology and demographics
- Glycogen storage disease type III historical perspective
- Glycogen storage disease type III history and symptoms
- Glycogen storage disease type III laboratory findings
- Glycogen storage disease type III medical therapy
- Glycogen storage disease type III MRI
- Glycogen storage disease type III natural history, complications and prognosis
- Glycogen storage disease type III other diagnostic studies
- Glycogen storage disease type III other imaging findings
- Glycogen storage disease type III overview
- Glycogen storage disease type III pathophysiology
- Glycogen storage disease type III physical examination
- Glycogen storage disease type III primary prevention
- Glycogen storage disease type III risk factors
- Glycogen storage disease type III screening
- Glycogen storage disease type III secondary prevention
- Glycogen storage disease type III surgery
- Glycogen storage disease type III x ray
- Glycogen storage disease type IV
- Glycogen storage disease type IX
- Glycogen storage disease type V
- Glycogen storage disease type VI
- Glycogen storage disease type VII
H
- Haemodialysis-associated amyloidosis
- Hexokinase deficiency
- High triglyceride life style modification
- Homocystinuria (patient information)
- Hunter syndrome (patient information)
- Hunter syndrome case study one
- Hurler syndrome (patient information)
- Hurler syndrome case study one
- Hurler syndrome classification
- Hyperglycemia
- Hyperinsulinemic hypoglycemia
- Hyperlipidemia historical perspective
- Hyperlipidemia NCEP guidelines for adjuvant therapies in children and adolescents