[2. Obesity due to overeating. Symptoms and classification of various forms of obesity].
Explore the source record for details and available documents.
Abnormalities, Multiple↗
Biomedical subjects
J Spranger
Publications and source records attributed to J Spranger.
[Congenital spondylo-epiphyseal dysplasia: follow-up of a case over 9 years (author's transl)].
A girl with the symptoms of dysplasia spondyloepiphysaria congenita has been observed during 9 years. The progressively severe alterations of the skeleton are demonstrated and briefly discussed.
Abnormalities, Multiple↗
Difficulties in the classification of the epiphyseal dysplasias.
Explore the source record for details and available documents.
Achondroplasia↗
The genetic mucolipidoses--definition and classification.
Explore the source record for details and available documents.
Aminoglycosides↗
Mannosidosis: clinical and biochemical findings.
Explore the source record for details and available documents.
Carbohydrate Metabolism, Inborn Errors↗
Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiency.
Explore the source record for details and available documents.
Carbohydrate Metabolism, Inborn Errors↗
Maroteaux-Lamy disease (mucopolysaccharidosis VI), subtype A: deficiency of a N-acetylgalactosamine-4-sulfatase.
Explore the source record for details and available documents.
Carbon Radioisotopes↗
A constitutional disorder of connective tissue suggesting a defect in collagen biosynthesis.
Explore the source record for details and available documents.
Biopsy↗
Mucopolysaccharidosis. VII. Beta-glucuronidase deficiency.
Explore the source record for details and available documents.
Child, Preschool↗
Short rib-polydactyly (SRP) syndromes, types Majewski and Saldino-Noonan.
Explore the source record for details and available documents.
Abnormalities, Multiple↗
[Possibilities of serum heterozygote tests in genetic mucopolysaccharidoses].
Explore the source record for details and available documents.
Female↗
Spondyloepiphyseal dysplasia.
Explore the source record for details and available documents.
Adolescent↗
Proceedings: The defect in Maroteaux-Lamy disease (mucopolysaccharidosis VI, subtype A): deficiency of N-acetylgalactosamine-4-sulfatase.
Explore the source record for details and available documents.
Acetylgalactosamine↗
Short rib-polydactyly syndromes and related conditions.
Explore the source record for details and available documents.
Abnormalities, Multiple↗
[Hereditary systemic diseases of the skeleton].
Explore the source record for details and available documents.
Achondroplasia↗
[Recent data on mucopolysaccharidoses].
Explore the source record for details and available documents.
Bone and Bones↗