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Papilledema in a toddler: An atypical presentation of X-linked hypophosphatemic rickets
Bone Abstracts
◽
10.1530/boneabs.4.p173
◽
2015
◽
Author(s):
Halley Wasserman
◽
Peggy Stenger
Keyword(s):
Hypophosphatemic Rickets
◽
Atypical Presentation
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Cited By
References
Primary hypophosphatemic rickets in an elderly woman
Archives of Internal Medicine
◽
10.1001/archinte.131.4.581
◽
1973
◽
Vol 131
(4)
◽
pp. 581-587
◽
Cited By ~ 1
Author(s):
V. Burnett
Keyword(s):
Elderly Woman
◽
Hypophosphatemic Rickets
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SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis
Yearbook of Endocrinology
◽
10.1016/s0084-3741(08)70143-4
◽
2007
◽
Vol 2007
◽
pp. 317-319
Author(s):
B.L. Clarke
Keyword(s):
Sodium Phosphate
◽
Hypophosphatemic Rickets
◽
Phosphate Homeostasis
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Hypophosphatemic Rickets: The Role of Hemiepiphysiodesis
Yearbook of Orthopedics
◽
10.1016/s0276-1092(08)70038-5
◽
2007
◽
Vol 2007
◽
pp. 35-36
Author(s):
H.A. Peterson
Keyword(s):
Hypophosphatemic Rickets
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Atypical Presentation of the GLUT-1 Deficiency Syndrome with Cataract and Normal Glucose Concentration in Cerebrospinal Fluid
Neuropediatrics
◽
10.1055/s-0034-1390645
◽
2014
◽
Vol 45
(S 01)
◽
Author(s):
N. Schmitz
◽
A. Blank
◽
M. Bartels
◽
R. König
◽
M. Kieslich
Keyword(s):
Cerebrospinal Fluid
◽
Glucose Concentration
◽
Deficiency Syndrome
◽
Atypical Presentation
◽
Glut 1
◽
Normal Glucose
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Elevated Creatinine Kinase in Connection with Wilson Disease: Atypical Presentation with Musculoskeletal Symptoms or Associated Neuromuscular Disease
Neuropediatrics
◽
10.1055/s-0036-1583658
◽
2016
◽
Vol 47
(S 01)
◽
Author(s):
N. Pfeifer
◽
Marina Della
◽
S. Kathemann
◽
B. Hegen
◽
S. Lutz
◽
...
Keyword(s):
Wilson Disease
◽
Neuromuscular Disease
◽
Creatinine Kinase
◽
Musculoskeletal Symptoms
◽
Atypical Presentation
◽
Elevated Creatinine
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Decision letter for "Functional Characterization of PHEX Gene Variants in Children with X‐linked Hypophosphatemic Rickets Shows no Evidence of Genotype‐Phenotype Correlation"
10.1002/jbmr.4035/v1/decision1
◽
2020
◽
Keyword(s):
Functional Characterization
◽
Hypophosphatemic Rickets
◽
Gene Variants
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ATYPICAL PRESENTATION OF SPINAL CORD TUMORS IN CHILDREN
Neuropediatrics
◽
10.1055/s-2006-945679
◽
2006
◽
Vol 37
(S 1)
◽
Author(s):
C Waisburg
◽
J Hukin
◽
F Durity
◽
E Roland
◽
A Hill
Keyword(s):
Spinal Cord
◽
Atypical Presentation
◽
Spinal Cord Tumors
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Atypical presentation of transverse myelitis in a 15 months old child
Neuropediatrics
◽
10.1055/s-2008-1079496
◽
2008
◽
Vol 39
(01)
◽
Author(s):
D Wüller
◽
B Köster
◽
T Rosenbaum
◽
H Alfke
Keyword(s):
Transverse Myelitis
◽
Atypical Presentation
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Acquired hypophosphatemic rickets in a 13-year-old boy presenting with knee pain and valgus deformity
Bone Abstracts
◽
10.1530/boneabs.2.p106
◽
2013
◽
Author(s):
Bowden Sasigarn
◽
Beebe Allan
◽
Wildman Sally
Keyword(s):
Knee Pain
◽
Valgus Deformity
◽
Hypophosphatemic Rickets
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Late onset autosomal dominant hypophosphatemic rickets; confirmation of the diagnosis with genomic analysis
Bone Abstracts
◽
10.1530/boneabs.1.pp5
◽
2013
◽
Author(s):
Symeon Tournis
◽
Ioannis Stathopoulos
◽
Kalliopi Lampropoulou-Adamidou
◽
Theodora Koromila
◽
Nikolaos Chatzistamatas
◽
...
Keyword(s):
Autosomal Dominant
◽
Late Onset
◽
Genomic Analysis
◽
Hypophosphatemic Rickets
◽
Autosomal Dominant Hypophosphatemic Rickets
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