Search Results - "Hoevenaars, F"

A case of Joubert's syndrome with extensive cerebral malformations by ten Donkelaar, H J, Hoevenaars, F, Wesseling, P

“…Joubert's syndrome is a relatively rare, autosomal-recessive syndrome defined by vermis hypoplasia, hypotonia, developmental delay and at least one of two…”
Get more information

Alpha- N-acetylgalactosaminidase deficiency with mild clinical manifestations and difficult biochemical diagnosis by de Jong, J., van den Berg, C., Wijburg, H., Willemsen, R., van Diggelen, O., Schindler, D., Hoevenaars, F., Wevers, R.

“…Two additional patients with α-N-acetylgalactosaminidase ( α-NAGA) deficiency are described. An 11-month-old girl with nonconsanguineous parents had…”
Get full text

Esophageal stricture as a complication in Henoch-Schönlein purpura by van Wieringen, P M, van der Zee, C L, Hoevenaars, F, Joosten, H J, Rieu, P N

“…We report on a three-year-old boy with Henoch-Schönlein purpura developing an esophageal stenosis during severe clinical course of this disease. There are to…”
Get more information

Acute polyarthritis in Mycoplasma pneumoniae infection by van Griethuysen, A J, van der Zee, C L, Hoevenaars, F

Get more information

Malignant hyperpyrexia: a frequently unrecognized complication of anesthesia by Hoevenaars, F, Sengers, R C, Stadhouders, A M, Gielen, M J, Brunings, W L, Trijbels, J M, Bookelman, H

Get more information