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Recommendations for the assessment and monitoring of skeletal manifestations in children with Gaucher disease

Author
MAAS, M1 ; HANGARTNER, T2 ; MARIANI, G3 ; MCHUGH, K4 ; MOORE, S5 ; GRABOWSKI, G. A6 7 ; KAPLAN, P8 ; VELLODI, A9 ; YEE, J10 ; STEINBACH, L11
[1] Department of Radiology, Suite G1-211, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, Netherlands
[2] BioMedical Imaging Laboratory, Wright State University and Miami Valley Hospital, Dayton, OH, United States
[3] Regional Center of Nuclear Medicine, University of Pisa, Pisa, Italy
[4] Department of Radiology, Great Ormond Street Hospital for Children, London, United Kingdom
[5] Department of Imaging Services, Children's Hospital of Los Angeles, Los Angeles, CA, United States
[6] Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
[7] Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States
[8] Department of Pediatrics, The Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA, United States
[9] Metabolic Unit, Great Ormond Street Hospital for Children, London, United Kingdom
[10] Global Medical Affairs, Genzyme Corporation, Cambridge, United States
[11] Department of Radiology, University of California San Francisco, San Francisco, CA, United States
Source

Skeletal radiology. 2008, Vol 37, Num 3, pp 185-188, 4 p ; ref : 10 ref

CODEN
SKRADI
ISSN
0364-2348
Scientific domain
Imagery; Orthopedics traumatology
Publisher
Springer, Berlin
Publication country
Germany
Document type
Article
Language
English
Keyword (fr)
Enfant Lipide Os Recommandation Sphingolipidose héréditaire de Gaucher Squelette Enzymopathie Homme Lipoïdose Maladie héréditaire Maladie métabolique Pathologie de l'encéphale Pathologie du système nerveux central Pathologie du système nerveux
Keyword (en)
Child Lipids Bone Recommendation Gaucher disease Skeleton Enzymopathy Human Lipoidosis Genetic disease Metabolic diseases Cerebral disorder Central nervous system disease Nervous system diseases
Keyword (es)
Niño Lípido Hueso Recomendación Esfingolipidosis hereditaria Gaucher Esqueleto Enzimopatía Hombre Lipoidosis Enfermedad hereditaria Metabolismo patología Encéfalo patología Sistema nervosio central patología Sistema nervioso patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D02 Lipids (lysosomal enzyme disorders, storage diseases)

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B24 Investigative techniques, diagnostic techniques (general aspects) / 002B24A Radiodiagnosis. Nmr imagery. Nmr spectrometry / 002B24A07 Osteoarticular system. Muscles

Discipline
Metabolic diseases Scanning and diagnostic techniques
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
20052973

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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