FAQ

Hyperphosphatasemia with bone disease

Known as: Familial Idiopathic Hyperphosphatasemia, Familial Osteoectasia, Chronic Congenital Idiopathic Hyperphosphatasemia 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1964-2018
02419642018

Related topics

Related topics

9 relations
AnkylosisAutosomal recessive inheritanceBowing of the long bonesDecalcification
(More)

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Hyperphosphatasemia with bone disease
Osteoporosis
Autosomal recessive inheritance
Sensorineural Hearing Loss (disorder)
Kyphosis deformity of spine
Osteitis Deformans

Papers overview

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2015
2015
Hypoxia-induced neuroinflammatory white-matter injury reduced by minocycline in SHR/SP.
Hypertensive small vessel disease is a major cause of vascular cognitive impairment (VCI). Spontaneously hypertensive/stroke… (More)
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2015
2015
Dynamic Uncertain Causality Graph for Knowledge Representation and Probabilistic Reasoning: Directed Cyclic Graph and Joint Probability Distribution
  • Qin Zhang
  • IEEE Transactions on Neural Networks and Learning…
  • 2015
Probabilistic graphical models (PGMs) such as Bayesian network (BN) have been widely applied in uncertain causality… (More)
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2014
2014
Tissue oxygen is reduced in white matter of spontaneously hypertensive-stroke prone rats: a longitudinal study with electron paramagnetic resonance.
Small vessel disease is associated with white-matter (WM) magnetic resonance imaging (MRI) hyperintensities (WMHs) in patients… (More)
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2013
2013
Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation.
Juvenile Paget's disease (JPD) is a rare heritable osteopathy characterized biochemically by markedly increased serum alkaline… (More)
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2010
2010
Profound hypocalcemia following effective response to zoledronic acid treatment in a patient with juvenile Paget’s disease
Juvenile Paget’s disease (JPD) is a rare, autosomal recessive osteopathy. Although it has phenotypic overlap with Paget’s disease… (More)
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2007
2007
Gender differences in endothelial function and inflammatory markers along the occurrence of pathological events in stroke-prone rats.
Spontaneously hypertensive stroke-prone rats (SHRSP) feature an established model for human cerebrovascular disease. SHRSP, kept… (More)
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2003
2003
Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype.
Homozygous mutations in TNFRSF11B, the gene encoding osteoprotegerin, were found in affected members from six of nine families… (More)
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1998
1998
Dopamine transporter density measured by [123I]beta-CIT single-photon emission computed tomography is normal in dopa-responsive dystonia.
The clinical distinction between dopa-responsive dystonia (DRD) and juvenile Parkinson's disease JPD) can pose a diagnostic… (More)
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1998
1998
The role of juxtapapillary duodenal diverticulum in the formation of gallbladder stones.
BACKGROUND/AIMS Juxtapapillary diverticula (JPD) are considered to be associated with choledocholithiasis but not with… (More)
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1996
1996
Juvenile Paget disease: life-long features of a mildly affected young woman.
Unusually mild Juvenile Paget Disease (JPD) was extensively investigated in a mentally retarded 21-year-old white woman… (More)
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