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Brain & Development|January 1, 1980
A form of congenital muscular dystrophyH H Goebel, H G Lenard, U Langenbeck, et al.
European Journal of Pediatrics|April 25, 1979
The development of skeletal muscles in premature infants. I. Fibre size and histochemical differentiationH Schloon, J Schlottmann, H G Lenard, et al.
Neuropediatrics|February 24, 1999
Complete remission of a diffuse pontine gliomaH G Lenard, V Engelbrecht, G Janssen, et al.
Quintessence International (Berlin, Germany : 1985)|November 1, 1995
Papillon-Lefèvre syndrome--successful treatment with a combination of retinoid and concurrent systematic periodontal therapy: case reportsS Kressin, A Herforth, S Preis, et al.
European Journal of Pediatrics|May 1, 1996
Goldenhar, Möbius and hypoglossia-hypodactyly anomalies in a patient: syndrome or association?S Preis, F Majewski, R Hantschmann, et al.
Electroencephalography and Clinical Neurophysiology|February 1, 1983
The EEG of mildly retarded children: developmental, classificatory, and topographic aspectsT Gasser, J Möcks, H G Lenard, et al.
European Journal of Pediatrics|September 1, 1994
Haemolytic anaemia in association with Escherichia coli O157 infection in two sistersC M Pennings, R C Seitz, H Karch, et al.
Pediatric Neurology|July 1, 1993
Pallister-Killian syndrome in older children and adolescentsG Horneff, F Majewski, B Hildebrand, et al.
Neuropediatrics|August 1, 1986
Hypomyelination neuropathy in a female newborn presenting as arthrogryposis multiplex congenitaR J Seitz, W Wechsler, D S Mosny, et al.
Pediatric Research|March 1, 1979
Rheologic properties of erythrocytes in Duchenne muscular dystrophyW Tillmann, H G Lenard, D Wagner, et al.
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