Paediatria Croatica - Volume

Volume: Vol. 47, No 2, april - june 2003

Motor neuron disease (MND) in a girl associated with neuropathy, mitochondrial abnormalities and centrometric deletion of survival motor neuron (smn) gene on chromosome 5q13
L. Brčić, N. Barišić, L. Pažanin, J. Sertić

Molecular update and therapeutic trials in muscle disorders of glycogen and lipid metabolism
C. Angelini

Neurologic phenotypes in tuberous sclerosis complex
P. Curatolo, M. Verdecchia, R. Bombardieri, N. Bottini

Fourteen-year follow up of a girl with primary systemic carnitine deficiency due to a carnitine transporter defect and OCTN2 mutation
Lj. Cvitanović-Šojat, I. Tein, A. M. Lamhonwah, L. De Meirleir, S. D. Cederbaum, Z. Jurčić, B. Mučić-Pucić, T. Lukanović-Novak

The Academy for developmental habilitation in Croatia
V. Mejaški Bošnjak

Neurological and cognitive outcome of extremely low birth weight (ELBW) and very low birth weight (VLBW) infants and two at four years of age
Modrušan Mozetič, I. Prpić, N. Sindičić Šimundić, I. Cicvarić Vlašić, E. Paučić Kirinčić

Risk registry of at-risk infants
Z. Modrušan Mozetič, M. Križ, E. Paučić Kirinčić, A. Sasso, I. Prpić, I. Vlašić Cicvarić

Quality of life in children and adolescents with epilepsy in Greece (pilot study)
I. Rizou, C. Kotsalis, C. Panou, P. Demakakos, A. Papavasiliou

Myoclonic astatic epilepsy of early childhood. Atypical benign partial epilepsy and pseudo Lennox syndrome - controversy in nosology
D. Škarpa, N. Barišić, M. Jurin. A. Bašnec, L. Brčić

Wildervanck syndrome (cervico-oculo-acoustic syndrome)
S. Čubelić, V. Mejaški Bošnjak, I. Borić, K. Rogulj