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Bilateral occipital calcification, epilepsy and coeliac disease: clinical and neuroimaging features of a new syndrome

Journal of neurology, neurosurgery and psychiatry, 1993-08, Vol.56 (8), p.885-889

1993

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Myoclonic encephalopathy in the CDKL5 gene mutation

Clinical neurophysiology, 2006, Vol.117 (1), p.223-227

2006

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Neurofibromatosis associated with central alveolar hypoventilation syndrome during sleep

Acta Paediatrica, 1994-07, Vol.83 (7), p.794-796

1994

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Microgyria associated with Sturge-Weber angiomatosis

Child's nervous system, 1994-08, Vol.10 (6), p.392-395

1994

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Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype

Journal of inherited metabolic disease, 1994-05, Vol.17 (3), p.301-303

1994

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Epilepsia partialis continua in a case of MELAS: Clinical and neurophysiological study

Neurophysiologie clinique, 1995, Vol.25 (3), p.158-166

1995

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Early myoclonic epileptic encephalopathy (E.M.E.E.)

European journal of pediatrics, 1983-01, Vol.140 (3), p.248-252

1983

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4p‐ Syndrome: A Chromosomal Disorder Associated with a Particular EEG Pattern

Epilepsia (Copenhagen), 1995-12, Vol.36 (12), p.1206-1214

1995

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Giant somatosensory evoked potentials and pathophysiology of hyperekplexia. Neurophysiological study of one patient

Neurophysiologie clinique, 1994-09, Vol.24 (4), p.318-324

1994

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Transient focal leukoencephalopathy following intraventricular methotrexate and cytarabine : a complication of the Ommaya reservoir : case report and review of the literature

Child's nervous system, 1990-06, Vol.6 (4), p.231-235

1990

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Sleep and benign partial epilepsies of childhood: EEG and evoked potentials study

Epilepsy research. Supplement, 1991, Vol.2, p.83

1991

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Status Epilepticus in Benign Rolandic Epilepsy Manifesting as Anterior Operculum Syndrome

Epilepsia (Copenhagen), 1991-06, Vol.32 (3), p.329-334

1991

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Kojewnikow's epilepsia partialis continua: Two cases associated with striatal necrosis

Neurophysiologie clinique, 1988-12, Vol.18 (6), p.525-530

1988

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Treatment with intravenously administered immunoglobulins of the neuroblastoma-associated opsoclonus-myoclonus

The Journal of pediatrics, 1996-07, Vol.129 (1), p.179-180

1996

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Progressive myoclonic encephalopathy in X-linked hypogamma-globulinemia. Case report, review of the literature and its relationship with progressive encephalopathy in children with A.I.D.S

Neuropediatrics, 1989-11, Vol.20 (4), p.223

1989

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Nosological classification of epilepsies in the first three years of life

Progress in clinical and biological research, 1983, Vol.124, p.165

1983

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Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua

Brain & development (Tokyo. 1979), 1996-05, Vol.18 (3), p.207-211

1996

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Epilepsy and disorders of cortical development in children with congenital cytomegalovirus infection

Revista de neurologiá, 1998-01, Vol.26 (149), p.42-49

1998

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Epilepsia y alteraciones del desarrollo cortical en niños con infección congénita por citomegalovirus

Revista de neurologiá, 1998, Vol.26 (149), p.42

1998

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Irreversible respiratory failure in an achondroplastic child: The importance of an early cervicomedullary decompression, and a review of the literature

Brain & development (Tokyo. 1979), 1991-07, Vol.13 (4), p.270-279

1991

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Epilepsie myoclonique grave de la premiere annee

Revue d'électroencéphalographie et de neurophysiologie clinique, 1982, Vol.12 (1), p.21-25

1982

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Muscle cytochromec oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype

Journal of inherited metabolic disease, 1994-05, Vol.17 (3), p.301-303

1994

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Tuberous sclerosis and down syndrome: A casual association?

Brain & development (Tokyo. 1979), 1992-07, Vol.14 (4), p.245-248

1992

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Biotin‐Responsive Infantile Encephalopathy: EEG‐Polygraphic Study of a Case

Epilepsia (Copenhagen), 1989-09, Vol.30 (5), p.573-578

1989

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Minipolymyoclonus in congenital nemaline myopathy: A nonspecific clinical marker of neurogenic dysfunction

Brain & development (Tokyo. 1979), 1991-09, Vol.13 (5), p.358-362

1991

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Bilateral occipital calcification, epilepsy and coeliac disease: clinical and neuroimaging features of a new syndrome

Myoclonic encephalopathy in the CDKL5 gene mutation

Neurofibromatosis associated with central alveolar hypoventilation syndrome during sleep

Microgyria associated with Sturge-Weber angiomatosis

Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype

Epilepsia partialis continua in a case of MELAS: Clinical and neurophysiological study

Early myoclonic epileptic encephalopathy (E.M.E.E.)

4p‐ Syndrome: A Chromosomal Disorder Associated with a Particular EEG Pattern

Giant somatosensory evoked potentials and pathophysiology of hyperekplexia. Neurophysiological study of one patient

Transient focal leukoencephalopathy following intraventricular methotrexate and cytarabine : a complication of the Ommaya reservoir : case report and review of the literature

Sleep and benign partial epilepsies of childhood: EEG and evoked potentials study

Status Epilepticus in Benign Rolandic Epilepsy Manifesting as Anterior Operculum Syndrome

Kojewnikow's epilepsia partialis continua: Two cases associated with striatal necrosis

Treatment with intravenously administered immunoglobulins of the neuroblastoma-associated opsoclonus-myoclonus

Progressive myoclonic encephalopathy in X-linked hypogamma-globulinemia. Case report, review of the literature and its relationship with progressive encephalopathy in children with A.I.D.S

Nosological classification of epilepsies in the first three years of life

Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilepsia partialis continua

Epilepsy and disorders of cortical development in children with congenital cytomegalovirus infection

Epilepsia y alteraciones del desarrollo cortical en niños con infección congénita por citomegalovirus

Irreversible respiratory failure in an achondroplastic child: The importance of an early cervicomedullary decompression, and a review of the literature

Epilepsie myoclonique grave de la premiere annee

Muscle cytochromec oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype

Tuberous sclerosis and down syndrome: A casual association?

Biotin‐Responsive Infantile Encephalopathy: EEG‐Polygraphic Study of a Case

Minipolymyoclonus in congenital nemaline myopathy: A nonspecific clinical marker of neurogenic dysfunction

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