General Introduction
- 1 May 1991
- journal article
- Published by Wiley in Acta Paediatrica
- Vol. 80 (s375), 5
- https://doi.org/10.1111/j.1651-2227.1991.tb12022.x
Abstract
No abstract availableKeywords
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- Neurological Findings in the Carbohydrate‐deficient Glycoprotein SyndromeActa Paediatrica, 1991
- Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome.Archives of Disease in Childhood, 1990
- Disialotransferrin developmental deficiency syndrome and olivopontocerebellar atrophy.Archives of Disease in Childhood, 1989
- A Newly Recognized Inherited Neurological Disease with Carbohydrate Deficient Secretory GlycoproteinsPublished by Springer Nature ,1989
- Disialotransferrin developmental deficiency syndrome.Archives of Disease in Childhood, 1989
- Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.Journal of Neurology, Neurosurgery & Psychiatry, 1988
- Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndromeClinica Chimica Acta; International Journal of Clinical Chemistry, 1984
- Familial psychomotor retardation with markedly fluctuating serum prolactin, FSH and GH levels, partial TBG-deficiency, increased serum arylsulphatase A and increased CSF protein: a new syndrome?: 90Pediatric Research, 1980