Lista de obras - Renata Rizzo - Dominio Público Uruguay

ADHD and Epilepsy in children with Tourette Syndrome: a triple comorbidity?

scientific article published on 27 September 2010

Aggressive behavior in patients with Sotos syndrome.

artículo científico publicado en 2000

Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection

artículo científico publicado en 2004

Association between D18S474 locus on chromosome 18q12 and idiopathic generalized epilepsy

artículo científico publicado en 2006

Association of Trp53 polymorphic variants at codon 72 with nonsyndromic mental retardation

artículo científico publicado en 2007

Association of adenosine deaminase polymorphism with mild mental retardation

artículo científico publicado en 2006

Autoimmune neuropsychiatric disorders associated with streptococcal infection: Sydenham chorea, PANDAS, and PANDAS variants

artículo científico publicado en 2006

Autosomal dominant and sporadic radio-ulnar synostosis.

artículo científico publicado en 1997

Autosomal-recessive microcephaly in two siblings, one with normal IQ and both with protruding mandible, small ears, and curved nose.

artículo científico publicado en 1995

Blink reflex abnormalities in children with Tourette syndrome

scientific article published on 01 August 2006

CSF N-glycan profile reveals sialylation deficiency in a patient with GM2 gangliosidosis presenting as childhood disintegrative disorder

artículo científico publicado en 2015

Cardiovascular safety of aripiprazole and pimozide in young patients with Tourette syndrome

artículo científico publicado en 2011

Circulating miRNAs profiles in Tourette syndrome: molecular data and clinical implications.

artículo científico publicado en 2015

Clinical correlates of quality of life in Tourette syndrome

artículo científico publicado en 2010

Clinical manifestations and evaluation of isolated lissencephaly

artículo científico publicado en 1993

Clinical pharmacology of comorbid attention deficit hyperactivity disorder in Tourette syndrome

artículo científico publicado en 2013

Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism

artículo científico publicado en 2004

Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism

artículo científico publicado en 1997

DNA repair investigations in nine Italian patients affected by trichothiodystrophy.

artículo científico publicado en 1992

Disease-specific quality of life in young patients with tourette syndrome

artículo científico publicado en 2013

Disentangling the effects of Tourette syndrome and attention deficit hyperactivity disorder on cognitive and behavioral phenotypes

artículo científico publicado en 2007

Erratum to: Long-term outcome of epilepsy in patients with Prader–Willi syndrome

artículo científico publicado en 2015

European clinical guidelines for Tourette Syndrome and other tic disorders. Part I: assessment ⬇️

artículo científico publicado el 1 de abril de 2011

Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome

artículo científico publicado en 2012

Familial broad terminal phalanges with one individual showing additional anomalies

artículo científico publicado en 1997

Familial broad terminal phalanges with one individual showing additional anomalies

Febrile and afebrile convulsions: a clinical follow-up

artículo científico publicado en 1993

Fragile X syndrome associated with tic disorders

artículo científico publicado en 2008

Genetic association signal near NTN4 in Tourette syndrome

artículo científico publicado en 2014

Guanfacine for the treatment of attention deficit hyperactivity disorder in children and adolescents

artículo científico

Hemihydranencephaly: living with half brain dysfunction

artículo científico publicado en 2013

Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy

artículo científico publicado en 2005

Incidence of Autism Spectrum Disorder in Youths Affected by Gilles de la Tourette Syndrome Based on Data from a Large Single Italian Clinical Cohort

artículo científico publicado en 2020

Increased antistreptococcal antibody titers and anti-basal ganglia antibodies in patients with Tourette syndrome: controlled cross-sectional study

artículo científico publicado en 2006

Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

artículo científico publicado en 2019

Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.

artículo científico publicado en 2014

Lack of Evidence for Association Between D2S124 and D2S111 Polymorphisms of the SCN2A Gene and Idiopathic Generalized Epilepsy With Generalized Tonic—Clonic Seizures

artículo científico publicado en 2007

Lateral dermoid cyst of the tongue: case report

scientific article published on 01 July 1994

Long term clinical course of Tourette syndrome

artículo científico publicado en 2011

Long-term neurological outcome of a sextuplet pregnancy.

artículo científico publicado en 2011

Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

artículo científico publicado en 2014

Mandatory electrocardiographic monitoring in young patients treated with psychoactive drugs

artículo científico publicado en 2013

Metabolic Effects of Aripiprazole and Pimozide in Children With Tourette Syndrome

scientific article published on 01 December 2012

Neuropsychological aspects of Tourette syndrome: a review

artículo científico publicado en 2009

New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement.

artículo científico publicado en 1992

Oculogyric crisis: a rare extrapyramidal side effect in the treatment of Tourette syndrome

artículo científico publicado en 2012

Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I.

artículo científico publicado en 1996

Parent and self-report health-related quality of life measures in young patients with Tourette syndrome

artículo científico publicado en 2012

Persistence in Therapy With Risperidone and Aripiprazole in Pediatric Outpatients: A 2-Year Naturalistic Comparison.

artículo científico publicado en 2016

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.

artículo científico publicado en 1999

Primary osteoma cutis — multiple café-au-lait spots and woolly hair anomaly

artículo científico publicado en 1995

Proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H): a model of a developmental field defect.

artículo científico publicado en 1995

Quality of life in young people with Tourette syndrome: a controlled study

artículo científico publicado en 2010

Quality of life in young people with treatment-responsive epilepsy: A controlled study

artículo científico publicado en 2010

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

artículo científico publicado en 2017

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.

artículo científico publicado en 2011

Second generation antipsychotics in 'real-life' paediatric patients. Adverse drug reactions and clinical outcomes of drug switch.

artículo científico publicado en 2016

Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families

artículo científico publicado en 2013

TBR1is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion

article

The Gilles de la Tourette Syndrome-Quality of Life Scale for children and adolescents (C&A-GTS-QOL): development and validation of the Italian version.

artículo científico publicado en 2013

The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients

The perception of time in childhood migraine

artículo científico publicado en 2014

The relationship between group A streptococcal infections and Tourette syndrome: a study on a large service-based cohort

artículo científico publicado en 2011

The successful use of ondansetron in a boy with both leukemia and Tourette syndrome

artículo científico publicado en 2008

Therapeutic drug monitoring of second-generation antipsychotics in pediatric patients: an observational study in real-life settings

artículo científico publicado en 2015

Three Cases of Palatal Tics and Gilles De La Tourette Syndrome

artículo científico

Timing recalibration in childhood Tourette syndrome associated with persistent pimozide treatment

artículo científico publicado en 2015

Tourette Syndrome and comorbid ADHD: current pharmacological treatment options

artículo científico publicado en 2013

Tourette syndrome and comorbid ADHD: causes and consequences.

artículo científico

Tourette syndrome and comorbid conditions: a spectrum of different severities and complexities

artículo científico publicado en 2014

Tourette syndrome: current data, comorbidities, and therapeutic approach in children

artículo científico publicado en 2014

Lista de obras de Renata Rizzo

ADHD and Epilepsy in children with Tourette Syndrome: a triple comorbidity?

Aggressive behavior in patients with Sotos syndrome.

Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection

Association between D18S474 locus on chromosome 18q12 and idiopathic generalized epilepsy

Association of Trp53 polymorphic variants at codon 72 with nonsyndromic mental retardation

Association of adenosine deaminase polymorphism with mild mental retardation

Autoimmune neuropsychiatric disorders associated with streptococcal infection: Sydenham chorea, PANDAS, and PANDAS variants

Autosomal dominant and sporadic radio-ulnar synostosis.

Autosomal-recessive microcephaly in two siblings, one with normal IQ and both with protruding mandible, small ears, and curved nose.

Blink reflex abnormalities in children with Tourette syndrome

CSF N-glycan profile reveals sialylation deficiency in a patient with GM2 gangliosidosis presenting as childhood disintegrative disorder

Cardiovascular safety of aripiprazole and pimozide in young patients with Tourette syndrome

Circulating miRNAs profiles in Tourette syndrome: molecular data and clinical implications.

Clinical correlates of quality of life in Tourette syndrome

Clinical manifestations and evaluation of isolated lissencephaly

Clinical pharmacology of comorbid attention deficit hyperactivity disorder in Tourette syndrome

Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism

Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism

DNA repair investigations in nine Italian patients affected by trichothiodystrophy.

Disease-specific quality of life in young patients with tourette syndrome

Disentangling the effects of Tourette syndrome and attention deficit hyperactivity disorder on cognitive and behavioral phenotypes

Erratum to: Long-term outcome of epilepsy in patients with Prader–Willi syndrome

European clinical guidelines for Tourette Syndrome and other tic disorders. Part I: assessment ⬇️

Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome

Familial broad terminal phalanges with one individual showing additional anomalies

Familial broad terminal phalanges with one individual showing additional anomalies

Febrile and afebrile convulsions: a clinical follow-up

Fragile X syndrome associated with tic disorders

Genetic association signal near NTN4 in Tourette syndrome

Guanfacine for the treatment of attention deficit hyperactivity disorder in children and adolescents

Hemihydranencephaly: living with half brain dysfunction

Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy

Incidence of Autism Spectrum Disorder in Youths Affected by Gilles de la Tourette Syndrome Based on Data from a Large Single Italian Clinical Cohort

Increased antistreptococcal antibody titers and anti-basal ganglia antibodies in patients with Tourette syndrome: controlled cross-sectional study

Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.

Lack of Evidence for Association Between D2S124 and D2S111 Polymorphisms of the SCN2A Gene and Idiopathic Generalized Epilepsy With Generalized Tonic—Clonic Seizures

Lateral dermoid cyst of the tongue: case report

Long term clinical course of Tourette syndrome

Long-term neurological outcome of a sextuplet pregnancy.

Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

Mandatory electrocardiographic monitoring in young patients treated with psychoactive drugs

Metabolic Effects of Aripiprazole and Pimozide in Children With Tourette Syndrome

Neuropsychological aspects of Tourette syndrome: a review

New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement.

Oculogyric crisis: a rare extrapyramidal side effect in the treatment of Tourette syndrome

Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I.

Parent and self-report health-related quality of life measures in young patients with Tourette syndrome

Persistence in Therapy With Risperidone and Aripiprazole in Pediatric Outpatients: A 2-Year Naturalistic Comparison.

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.

Primary osteoma cutis — multiple café-au-lait spots and woolly hair anomaly

Proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H): a model of a developmental field defect.

Quality of life in young people with Tourette syndrome: a controlled study

Quality of life in young people with treatment-responsive epilepsy: A controlled study

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.

Second generation antipsychotics in 'real-life' paediatric patients. Adverse drug reactions and clinical outcomes of drug switch.

Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families

TBR1is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion

The Gilles de la Tourette Syndrome-Quality of Life Scale for children and adolescents (C&A-GTS-QOL): development and validation of the Italian version.

The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients

The perception of time in childhood migraine

The relationship between group A streptococcal infections and Tourette syndrome: a study on a large service-based cohort

The successful use of ondansetron in a boy with both leukemia and Tourette syndrome

Therapeutic drug monitoring of second-generation antipsychotics in pediatric patients: an observational study in real-life settings

Three Cases of Palatal Tics and Gilles De La Tourette Syndrome

Timing recalibration in childhood Tourette syndrome associated with persistent pimozide treatment

Tourette Syndrome and comorbid ADHD: current pharmacological treatment options

Tourette syndrome and comorbid ADHD: causes and consequences.

Tourette syndrome and comorbid conditions: a spectrum of different severities and complexities

Tourette syndrome: current data, comorbidities, and therapeutic approach in children