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Severe infantileBordetella pertussispneumonia in monozygotic twins with a congenital C3 deficiency

✍ Scribed by Kurvers, Roel A. J.; Westra, Dineke; van Heijst, Arno F.; Walk, Twiggy L. M.; Warris, Adilia; van de Kar, Nicole C. A. J.


Book ID
125347503
Publisher
Springer
Year
2013
Tongue
English
Weight
267 KB
Volume
173
Category
Article
ISSN
0340-6997

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Congenital ocular motor apraxia associat
✍ J A Gonzalez-Martin; L C Kaye; M Brown; I Ellis; R Appelton; S B Kaye πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 151 KB

Identical female twins (age 11 years) with congenital ocular motor apraxia and generalized idiopathic epilepsy are reported. Their presenting symptoms were a long history of abnormal head and eye movements. One twin developed partial sensory seizures. The patients underwent 16-channel EEG, electro-o