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Hyperphosphatasemia with bone disease
Known as:
Familial Idiopathic Hyperphosphatasemia
, Familial Osteoectasia
, Chronic Congenital Idiopathic Hyperphosphatasemia
Â
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National Institutes of Health
Topic mentions per year
Topic mentions per year
1964-2018
0
2
4
1964
2018
Related topics
Related topics
9 relations
Ankylosis
Autosomal recessive inheritance
Bowing of the long bones
Decalcification
(More)
Related mentions per year
Related mentions per year
1936-2018
1940
1960
1980
2000
2020
Hyperphosphatasemia with bone disease
Osteoporosis
Autosomal recessive inheritance
Sensorineural Hearing Loss (disorder)
Kyphosis deformity of spine
Osteitis Deformans
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Hypoxia-induced neuroinflammatory white-matter injury reduced by minocycline in SHR/SP.
Fakhreya Yousuf Jalal
,
Yi Yang
,
Jeffrey F. Thompson
,
Tamara Roitbak
,
Gary A Rosenberg
Journal of cerebral blood flow and metabolism…
2015
Hypertensive small vessel disease is a major cause of vascular cognitive impairment (VCI). Spontaneously hypertensive/stroke…Â
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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…Â
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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.
John Weaver
,
Fakhreya Yousuf Jalal
,
Yi Yang
,
Jeffrey Thompson
,
Gary A Rosenberg
,
Ke Liu
Journal of cerebral blood flow and metabolism…
2014
Small vessel disease is associated with white-matter (WM) magnetic resonance imaging (MRI) hyperintensities (WMHs) in patients…Â
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2013
2013
Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation.
Forough Saki
,
Zohreh Karamizadeh
,
Shiva Nasirabadi
,
Steven R. Mumm
,
W H Mcalister
,
Michael P Whyte
Journal of bone and mineral research : the…
2013
Juvenile Paget's disease (JPD) is a rare heritable osteopathy characterized biochemically by markedly increased serum alkaline…Â
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2010
2010
Profound hypocalcemia following effective response to zoledronic acid treatment in a patient with juvenile Paget’s disease
Stergios A Polyzos
,
Athanasios D. Anastasilakis
,
+6 authors
Evangelos Terpos
Journal of Bone and Mineral Metabolism
2010
Juvenile Paget’s disease (JPD) is a rare, autosomal recessive osteopathy. Although it has phenotypic overlap with Paget’s disease…Â
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2007
2007
Gender differences in endothelial function and inflammatory markers along the occurrence of pathological events in stroke-prone rats.
Rossana Ballerio
,
Elisabetta Gianazza
,
+8 authors
Luigi Sironi
Experimental and molecular pathology
2007
Spontaneously hypertensive stroke-prone rats (SHRSP) feature an established model for human cerebrovascular disease. SHRSP, kept…Â
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2003
2003
Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype.
B. Chong
,
Madhuri R. Hegde
,
+10 authors
T. P. Cundy
Journal of bone and mineral research : the…
2003
Homozygous mutations in TNFRSF11B, the gene encoding osteoprotegerin, were found in affected members from six of nine families…Â
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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.
B. S. Jeon
,
J M Jeong
,
+7 authors
S. B. Lee
Annals of neurology
1998
The clinical distinction between dopa-responsive dystonia (DRD) and juvenile Parkinson's disease JPD) can pose a diagnostic…Â
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1998
1998
The role of juxtapapillary duodenal diverticulum in the formation of gallbladder stones.
Naohiro Egawa
,
Terumi Kamisawa
,
Y Tu
,
Naoyoshi Sakaki
,
K.. Tsuruta
,
Atsuko Okamoto
Hepato-gastroenterology
1998
BACKGROUND/AIMS Juxtapapillary diverticula (JPD) are considered to be associated with choledocholithiasis but not with…Â
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1996
1996
Juvenile Paget disease: life-long features of a mildly affected young woman.
D S Golob
,
W H Mcalister
,
+5 authors
Martin Whyte
Journal of bone and mineral research : the…
1996
Unusually mild Juvenile Paget Disease (JPD) was extensively investigated in a mentally retarded 21-year-old white woman…Â
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