A. Diament

发表

Discontinuing Medication in Epileptic Children: A Study of Risk Factors Related to Recurrence

F. Kok, J. Gherpelli, B. Lefèvre, 1992, Epilepsia.

Seizure recurrence in infants with neonatal convulsions. A follow-up study.

J. Paz, J. Gherpelli, C. Leone, 1992, Arquivos de neuro-psiquiatria.

Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients.

M. Varela, C. Koiffmann, F. Kok, 2000, American journal of medical genetics.

Heterogeneity of Classic Congenital Muscular Dystrophy With Involvement of the Central Nervous System: Report of Five Atypical Cases

M. Zatz, M. Resende, U. Reed, 2000, Journal of child neurology.

Multiple sclerosis with early childhood onset. A case report.

R. Reimão, A. M. Silva, M. Muskat, 1988, Arquivos de neuro-psiquiatria.

Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency

M. Zatz, U. Reed, M. Vainzof, 1996, Brain and Development.

Neonatal Mass Screening of Hereditary Metabolic Diseases in S. Paulo‐Brasil

M. M. Rodrígues, A. Diament, B. Schmidt, 1980 .

King-Denborough Syndrome: report of two Brazilian cases.

U. Reed, M. Scaff, S. Marie, 2002, Arquivos de neuro-psiquiatria.

Macrocephaly, multiple lipomas, and hemangiomata (Bannayan-Zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms?

D. Moretti-Ferreira, C. Koiffmann, A. Wajntal, 1989, American journal of medical genetics.

Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation

U. Reed, M. Vainzof, S. Marie, 1999, Brain and Development.

A pilot study of topiramate in children with Lennox-Gastaut syndrome.

U. Reed, J. Bacaltchuk, H. Chiu, 1999, Arquivos de neuro-psiquiatria.

Treatment of febrile seizures with intermittent clobazam.

M. Manreza, J. Gherpelli, C. Heise, 1997, Arquivos de neuro-psiquiatria.

Evolução neurológica de crianças de baixo peso ao nascimento Neurological evolution of children with lowbirth weight

A. Diament, Rosi M. Grossmann, C. G. Deluqui, 1976 .

Nevos sebáceo linear de Jadassohn: registro de um caso

A. Diament, P. Campos-Olazabal, R. F. Espinoza, 1982 .

Intracranial abscesses in infancy and childhood: report of 40 cases.

R. Reimão, A. Diament, T. D. Oliveira, 1984, Arquivos de neuro-psiquiatria.

Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11.

S. Kihara, C. Koiffmann, A. Wajntal, 1993, American journal of medical genetics.

Schwartz-Jampel syndrome: report of five cases.

U. Reed, M. Scaff, R. Reimão, 2002, Arquivos de neuro-psiquiatria.

Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.

M. Zatz, A. Vianna-Morgante, A. Diament, 1981, Journal of medical genetics.

Median cleft face syndrome or frontonasal dysplasia: a case report with associated kidney malformation.

A. Wajntal, A. Diament, J. Roizenblatt, 1979, Journal of pediatric ophthalmology and strabismus.

Ring chromosome 7 in a man with multiple congenital anomalies and mental retardation.

C. Koiffmann, A. Wajntal, D. H. de Souza, 1990, Journal of medical genetics.

A ring D chromosome in association with Down's syndrome-like phenotype.

P. H. Saldanha, A. Wajntal, A. Diament, 1973, Arquivos de neuro-psiquiatria.

In search of a genetic basis for the Rett syndrome

M. J. Marques-Dias, F. Kok, C. Gonzalez, 1990, Human Genetics.

Periodic hypersomnia, congenital ectodermal disorders and multiple exostosis.

R. Reimão, A. Diament, 1989, Arquivos de neuro-psiquiatria.

Follow-up study of macrocephalic children with enlargement of the subarachnoid space.

M. Manreza, J. Gherpelli, A. Diament, 1992, Arquivos de neuro-psiquiatria.

DOPA-sensitive progressive dystonia of childhood with diurnal fluctuations of symptoms: a case report.

L. Nagae, J. Gherpelli, A. Diament, 1995, Arquivos de neuro-psiquiatria.

Hyperekplexia, a cause of neonatal apnea: a case report

E. Troster, C. Leone, A. Diament, 1995, Brain and Development.

Pediatric multiple sclerosis report of 14 cases

L. Guilhoto, M. Manreza, F. Kok, 1995, Brain and Development.

Episodic somnolence in an infant with Riley-Day syndrome.

E. Casella, A. Bousso, A. Diament, 2005, Pediatric neurology.

[Menkes syndrome: review of the pathogenesis apropos of a clinico-pathological case].

U. Reed, M. Scaff, S. Rosemberg, 1984, Arquivos de neuro-psiquiatria.

Subacute sclerosing panencephalitis. Clinical aspects and prognosis. The Brazilian registry.

J. D. da Costa, M. Nunes, S. Rosemberg, 1999, Arquivos de neuro-psiquiatria.

[Syndrome of calcifications of basal ganglia, leukodystrophy and chronic lymphomonocytic pleocytosis of the cerebrospinal fluid: report of a case].

S. Cypel, J. Ramos, A. Diament, 1986, Arquivos de neuro-psiquiatria.

Anemia de Fanconi: relato de dois casos na mesma família

R. Reimão, A. Diament, Rubens Reimão, 1983 .