A gene for ataxic cerebral palsy maps to chromosome 9p12–q12

No abstract is available for this paper.

• Publication year

  2000

• Venue

  European Journal of Human Genetics

• Publication date

  2000-04-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/sj.ejhg.5200445PMID 10854109
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Neurology of the newborn.

  2013cited by this paper
• Recent advances: Paediatrics

  2001cited by this paper
• Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.

  1997cited by this paper
• Prevalence and type of cerebral palsy in a British ethnic community: the role of consanguinity

  1997cited by this paper
• A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands.

  1996cited by this paper
• Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

  1996cited by this paper
• Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.

  1995cited by this paper
• Early‐onset ataxia with cardiomyopathy and retained tendon reflexes maps to the friedreich's ataxia locus on chromosome 9q

  1995cited by this paper
• Complete block of early B cell differentiation and altered patterning of the posterior midbrain in mice lacking Pax5/BSAP.

  1994cited by this paper
• Genetic Aspects of Cerebral Palsy

  1992cited by this paper
• An Extended Phenotype of an Early-Onset Inherited Nonprogressive Cerebellar Ataxia Syndrome

  1991cited by this paper
• Conservation of the paired domain in metazoans and its structure in three isolated human genes.

  1989cited by this paper
• Sex-linked recessive congenital ataxia.

  1987cited by this paper
• The Hereditary Ataxias and Related Disorders

  1986cited by this paper
• Birth and the origins of cerebral palsy.

  1986cited by this paper
• Easy calculations of lod scores and genetic risks on small computers.

  1984cited by this paper
• Human cerebellar hypoplasia: a syndrome of diverse causes.

  1980cited by this paper
• Recurrence Risks in Families of Children with Symmetrical Spasticity

  1977cited by this paper
• The Dysequilibrium Syndrome – A genetic study

  1973cited by this paper
• The dysequilibrium syndrome in cerebral palsy. Clinical aspects and treatment.

  1972cited by this paper
• IDENTICAL SYNDROMES OF CEREBRAL PALSY IN THE SAME FAMILY

  1969cited by this paper
• Congenital Ataxic Syndromes in Cerebral Pals 1

  1962cited by this paper

• Cerebral palsy as a childhood-onset neurological disorder caused by both genetic and environmental factors.

  2024cites this paper
• Clinical Characteristics Suggestive of a Genetic Cause in Cerebral Palsy: A Systematic Review.

  2024cites this paper
• Effects of a core stability exercise program on balance and coordination in children with cerebellar ataxic cerebral palsy

  2022cites this paper
• Clinical overview and phenomenology of movement disorders

  2021cites this paper
• A Review on the Types, Risk Factors, Diagnosis, and Treatment of Cerebral Palsy

  2021cites this paper
• Clinical patterns of Cerebral palsy in children who underwent serial casting for improvement in mobility at a tertiary care centre

  2021cites this paper
• Genome-Wide Association Study Identifies Genetic Risk Factors for Spastic Cerebral Palsy.

  2021cites this paper
• Trunk Control in Children With Ataxic Cerebral Palsy

  2019cites this paper
• Epilepsy in children with cerebral palsy

  2019cites this paper
• Possible neurogenic disorder in a female buried in the monastic cemetery at Ghazali (ca. 670–1270 CE), northern Sudan

  2019cites this paper
• Establish Registry of Cerebral Palsy in Qalubia Goveronrate

  2019cites this paper
• Profile of children with cerebral palsy spectrum disorder and a normal MRI study

  2019cites this paper
• Establish Registry of Cerebral Palsy in Suez Governorate

  2018cites this paper
• Cerebellar motor syndrome from children to the elderly.

  2018cites this paper
• Cerebral Palsy: A Webliography

  2018cites this paper
• Cerebral Palsy—Trends in Epidemiology and Recent Development in Prenatal Mechanisms of Disease, Treatment, and Prevention

  2017cites this paper
• Global distribution of consanguinity and their impact on complex diseases: Genetic disorders from an endogamous population

  2017cites this paper
• ESTABLISH REGISTRY OF CEREBRAL PALSY IN TANTA EGYPT

  2017cites this paper
• Cerebellar transcranial direct current stimulation in children with ataxic cerebral palsy: A sham-controlled, crossover, pilot study

  2017cites this paper
• Antibody responses to botulinum neurotoxin type A of toxin-treated spastic equinus children with cerebral palsy: A randomized clinical trial comparing two injection schedules.

  2017cites this paper
• Evaluation du niveau de traitement des enfants polyhandicapés hospitalisés en urgence en réanimation médicale pédiatrique en île de France

  2017cites this paper
• Genetic Aspect of Cerebral palsy on the Basis of Quantitative Analysis in Digitopalmar Dermatoglyphycs of Eighty Six Female Children

  2017cites this paper
• Antecedents of Cerebral Palsy in children born at term - according to subtype, motor severity and accompanying impairments

  2016cites this paper
• Association of COL4A1 gene polymorphisms with cerebral palsy in a Chinese Han population

  2016cites this paper
• The importance of de novo mutations for pediatric neurological disease--It is not all in utero or birth trauma.

  2016cites this paper
• Candidate single-nucleotide polymorphisms and cerebral palsy: A case-control study.

  2015cites this paper
• A Diagnostic Approach for Cerebral Palsy in the Genomic Era

  2014cites this paper
• Gene sequences regulating the production of apoE and cerebral palsy of variable severity.

  2014influential citation
• A Tale of Two Boys: Case Report on Non- Consanguineous Siblings with Cerebral Palsy

  2014cites this paper
• Incidence of Cerebral Palsy in Yorkshire by ethnicity and area deprivation

  2013cites this paper
• Normal imaging in patients with cerebral palsy: what does it tell us?

  2013cites this paper
• The association between GAD1 gene polymorphisms and cerebral palsy in Chinese infants

  2013cites this paper
• Genetic association study of adaptor protein complex 4 with cerebral palsy in a Han Chinese population

  2013cites this paper
• Rare copy number variation in cerebral palsy

  2013cites this paper
• Social, Environmental and Biological Determinants of Cerebral Palsy in Children with Intellectual Disabilities (ID) in India

  2013cites this paper
• 2 CONSANGUINEOUS MARRIAGES AND THEIR EFFECT ON COMMON DISEASES IN THE QATARI POPULATION

  2012cites this paper
• AN AYURVEDIC PERSPECTIVE TOWARDS CEREBRAL PALSY

  2012cites this paper
• Chapter 1 – Clinical overview and phenomenology of movement disorders

  2011cites this paper
• Risk factors for cerebral palsy in children born at term

  2011cites this paper
• Adult-onset cerebellar Ataxia: a clinical and genetic Survey

  2011cites this paper
• Molecular Genetics and Fetal Brain

  2008cites this paper
• Molecular Genetics and Fetal Brain

  2008cites this paper
• Genetics considerations in cerebral palsy.

  2008cites this paper
• Linkage Analysis in a Large Family from Pakistan with Depression and a High Incidence of Consanguineous Marriages

  2008cites this paper
• Consanguineous Marriages and Their Effects on Common Adult Diseases: Studies from an Endogamous Population

  2007cites this paper
• Study of Gene Expression Profiles and Biological Mechanism of Cerebral Palsy Using a Monozygotic Twin Pair

  2007cites this paper
• Autosomal recessive cerebellar hypoplasia in the Hutterite population.

  2005cites this paper
• Autosomal recessive cerebellar hypoplasia in the Hutterite population

  2005cites this paper
• Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders

  2004cites this paper
• A new locus for a childhood onset, slowly progressive autosomal recessive spinocerebellar ataxia maps to chromosome 11p15

  2004cites this paper
• Parálisis cerebral: nuevos conceptos etiopatogénicos

  2003cites this paper
• Consanguineous marriage and childhood health

  2003cites this paper
• [Cerebral palsy: new pathogenetic concepts].

  2003cites this paper
• Cloning and characterization of a novel human gene RNF38 encoding a conserved putative protein with a RING finger domain.

  2002cites this paper
• Intellectual Disability and Cerebral Palsy in a UK Community

  2002cites this paper
• Paternal factors and schizophrenia risk: de novo mutations and imprinting.

  2001cites this paper
• Ataxias of Childhood

  2001cites this paper