[Mucolipidosis Type II. STudy of 2 familial cases. Clinical and biochemical aspects]
[Article in
French]
- PMID: 4218311
Item in Clipboard
[Mucolipidosis Type II. STudy of 2 familial cases. Clinical and biochemical aspects]
[Article in
French]
Pediatrie.
1974 Dec.
No abstract available
Similar articles
-
[Hunter's disease: genetic, clinical and biochemical study of a new family].Acta Neurol Quad (Napoli). 1979;39:90-100. Acta Neurol Quad (Napoli). 1979. PMID: 162337 Italian. No abstract available.
-
[Mucopolysaccharidosis type II (Hurler-Hunter) in siblings. Electron microscopic study].Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove. 1972;15(2):173-9. Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove. 1972. PMID: 4209410 German. No abstract available.
-
[Multiple deformities of a compressive nature in a full-term newborn infant].Chir Organi Mov. 1975;62(3):325-9. Chir Organi Mov. 1975. PMID: 1222605 Italian. No abstract available.
-
Prenatal diagnosis of right pulmonary agenesis associated with VACTERL sequence.Prenat Diagn. 2003 Jun;23(6):515-8. doi: 10.1002/pd.615. Prenat Diagn. 2003. PMID: 12813771 Review. No abstract available.
-
Genetic and environmental factors in profound prelingual deafness.Med Clin North Am. 1969 Jul;53(4):741-72. Med Clin North Am. 1969. PMID: 4894100 Review. No abstract available.
Cited by
-
Mucolipidosis II: correlation between radiological features and histopathology of the bones.Pediatr Radiol. 1989;19(6-7):406-13. doi: 10.1007/BF02387638. Pediatr Radiol. 1989. PMID: 2771479
-
Radiological signs of mucolipidosis II or I-cell disease. A study of nine cases.Pediatr Radiol. 1978 Jun 19;7(2):97-105. doi: 10.1007/BF00975678. Pediatr Radiol. 1978. PMID: 673536
-
Neonatal mucolipidosis 2. The spontaneous evolution of early bone lesions and the effect of vitamin D treatment. Report of two cases.Pediatr Radiol. 1989;20(1-2):80-4. doi: 10.1007/BF02010640. Pediatr Radiol. 1989. PMID: 2602022