Amelogenesis Imperfecta, Type IB

Known as: AIH2, Amelogenesis Imperfecta, Hypoplastic Local, Autosomal Dominant, Enamel Hypoplasia, Hereditary Localized 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2015
01219962015

Papers overview

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2015
2015
An association of human leukocyte antigen (HLA) class II alleles with autoimmune conditions is increasingly being used for… (More)
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Review
2015
Review
2015
BACKGROUND Little is known about autoimmune liver disease (AILD) in Asian children. We studied the clinical features and… (More)
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Review
2010
Review
2010
BACKGROUND Graft rejection and disease recurrence are well-recognized complications of liver transplantation (LT) for autoimmune… (More)
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2007
2007
Amelogenesis imperfecta is an inherited disorder affecting tooth enamel formation. We previously isolated a mouse strain with an… (More)
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2002
2002
Amelogenesis imperfecta (AI) is an inherited tooth disorder affecting tooth enamel formation only. A gene for autosomal dominant… (More)
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2001
2001
A gene encoding the enamel protein ameloblastin (AMBN) was recently localized to a region on chromosome 4q21 containing a gene… (More)
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Review
2001
Review
2001
A detailed study of the mechanism by which a proton is lost from a dication reveals that such processes are more complicated than… (More)
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1997
1997
Amelogenesis imperfecta (AI) is a broad group of hereditary enamel defects that is characterized by a high degree of clinical… (More)
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1997
1997
Amelogenesis imperfecta (AI) is a clinically and genetically heterogeneous group of inherited enamel defects. We recently mapped… (More)
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1996
1996
Amelogenesis imperfecta (AI) is a group of hereditary enamel defects, characterized by large clinical diversity. On the basis of… (More)
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