Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder. - Test2 - elhamkhani - TriplyDB

Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder.

Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder.

http://www.wikidata.org/entity/Q33926696

about

Neuropathology and animal models of autism: genetic and environmental factors Sequencing the unsequenceable: expanded CGG-repeat alleles of the fragile X gene Mouse Genetic Models of Human Brain Disorders Advances in the Understanding of the Gabaergic Neurobiology of FMR1 Expanded Alleles Leading to Targeted Treatments for Fragile X Spectrum Disorder Fragile X spectrum disorders Fragile X-associated tremor/ataxia syndrome.Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders NINDS epilepsy and autism spectrum disorders workshop report Advanced technologies for the molecular diagnosis of fragile X syndrome Phenobarbital use and neurological problems in FMR1 premutation carriers Neuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum Disorders CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles.Early identification of autism in fragile X syndrome: a review.FMR1 premutation with Prader-Willi phenotype and fragile X-associated tremor/ataxia syndrome.Epilepsy drives autism in neurodevelopmental disorders.FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States Towards an Understanding of Neuropsychiatric Manifestations in Fragile X Premutation Carriers Associated features in females with an FMR1 premutation A hypothesis regarding the molecular mechanism underlying dietary soy-induced effects on seizure propensity Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers Addictive substances may induce a rapid neurological deterioration in fragile X-associated tremor ataxia syndrome: A report of two cases PSYCHIATRIC DISORDERS ASSOCIATED WITH FXTAS.Abnormal dendrite and spine morphology in primary visual cortex in the CGG knock-in mouse model of the fragile X premutation Dysregulated iron metabolism in the choroid plexus in fragile X-associated tremor/ataxia syndrome Psychosis and catatonia in fragile X: Case report and literature review.Clustered burst firing in FMR1 premutation hippocampal neurons: amelioration with allopregnanolone.Anxiety disorders in fragile X premutation carriers: Preliminary characterization of probands and non-probands.Current Gaps in Understanding the Molecular Basis of FXTAS Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study.Identification of a male with fragile X syndrome through newborn screening TARGETED TREATMENTS IN AUTISM AND FRAGILE X SYNDROME Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.Influence of the fragile X mental retardation (FMR1) gene on the brain and working memory in men with normal FMR1 alleles.Fragile X syndrome: an aging perspective.Prevalence and risk of migraine headaches in adult fragile X premutation carriers Developmental profiles of infants with an FMR1 premutation.Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms.Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome.Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptions.Development of mavoglurant and its potential for the treatment of fragile X syndrome.

P2860

Q21284779-2E14D0CD-53D9-4469-BCB6-442C036953CF Q24596776-244B7DBC-6E70-43EB-99C0-9126CF6B3782 Q26752246-4DC05F88-47CD-4182-8B99-3883E8944090 Q26781265-AE86FAA1-B16B-442A-B3CE-AC84BB270170 Q26824376-DB21608E-E62D-4CA6-AAD1-B6D4E0BA699F Q26852667-62B67F48-079F-490D-AF6B-95BDEE4A0F71 Q27011565-F1A285F8-3BD0-4169-AFE3-E4E497325966 Q27022529-220D0C7C-94FC-46C8-80D8-88E883F433C6 Q28087781-2BCECC13-6E14-4FF9-9155-DF062A64D3D1 Q28390629-A20C1010-56CE-44DA-A08B-1EE0174B2D34 Q28396205-5B5B721F-C94B-47B3-A2AF-1D46BA723CCA Q33567772-BF8F1A7A-C908-4EFE-9999-6A0C37232715 Q33620669-DCF1BC0F-0F95-43AE-BDB4-940AF052DC6B Q33625894-174C5C57-5814-4CA0-B913-EA79FD2FE30B Q33733577-B7892A87-5053-42D4-9381-D47EF15524A3 Q33781086-A380A12D-DA09-40B3-BF02-F9180D9AC49E Q33863331-CC55A597-011B-436A-918C-3370DB614B44 Q34000722-2ECBAD77-0BD0-409A-B932-5EEC5FAC11AD Q34125778-5AF91513-6929-4A77-965A-1B7C172006E9 Q34575595-4112A3D4-F50B-4A2A-B0E5-5406501B8560 Q34983521-42F7EC68-BB4D-4451-92C8-8E5EF5F39462 Q35006614-43BA0B5A-688B-48E1-85B7-4CD8C473CDC9 Q35047721-E0A6A534-528E-47F9-859F-88511EFFA6A5 Q35122403-CBE70B61-2A30-46C2-8B99-7FA457CBEF8B Q35771116-5391A7F7-67C4-4C0B-92B3-70BDBC25C1A7 Q36026897-CACE3FB5-34FD-4A4A-BC61-B886A963C211 Q36031757-0E9567BA-28BE-4AE8-93AE-A5EDF5C80F15 Q36048562-9016461E-10FD-49E6-B30E-6B2B771EA566 Q36132963-C782E7C2-C4BA-45FF-8E43-1991DE6976BD Q36322068-DC036CA4-0DE1-4E94-AB24-C76E595183D6 Q36399716-0CA33178-ACD2-4FDD-BA03-4022556436CF Q36498006-91B9FCD5-0752-4677-85B7-1EBFF7500AC0 Q36518325-37DE7374-316F-4C8A-81F2-A90ABC8D52B6 Q37122910-54886C00-AC72-4D5B-A9B0-9F867C7443A9 Q37191145-9C11360B-3C37-4F78-B470-7DAD04D37D80 Q37394408-2562297A-EFE7-4DA7-A8E8-E42C4BB7FC07 Q37524454-05F1C764-802D-4D48-8EB2-A358A1AF0B71 Q37580522-CEC0A792-868F-4784-B99B-E9EE0114C9F7 Q37730919-5FA9B619-929A-498C-B592-79F315C3153A Q38164021-57C2A6C0-BC94-4514-BEE8-0F0C23D74A05

P2860

Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder.

http://www.wikidata.org/entity/Q33926696

description

2011 nî lūn-bûn

@nan

2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Increased prevalence of seizur ...... rbid autism spectrum disorder.

@ast

Increased prevalence of seizur ...... rbid autism spectrum disorder.

@en

type

label

Increased prevalence of seizur ...... rbid autism spectrum disorder.

@ast

Increased prevalence of seizur ...... rbid autism spectrum disorder.

@en

prefLabel

Increased prevalence of seizur ...... rbid autism spectrum disorder.

@ast

Increased prevalence of seizur ...... rbid autism spectrum disorder.

@en

P1433

Q33926696-C98C77D9-79D6-4A38-84A3-39ADC05E8E2B

P1476

Q33926696-C58B7A1D-1710-4C07-9002-E1A456FB3110

P2093

Q33926696-5E1DF395-8B97-4AB5-83B8-32E395356508

Q33926696-6CB0DFA7-6214-4A33-AD73-B0552CEA1C8C

Q33926696-6ED97E05-BEAF-4161-847E-34D2E21FBB8B

Q33926696-71411C29-7E6C-4698-9E39-90507AFBDAA3

Q33926696-95E60555-1030-4601-9E28-C8189F264A9E

Q33926696-962FFC76-22BA-41AA-B59C-7301BA7DEAD4

Q33926696-C4D93ADF-7082-4153-9888-639EAD4BD592

Q33926696-C8C23B23-7F9E-4969-B4D2-73D4CCFE5A70

P2860

Q33926696-047D5AA0-C950-4A43-A9F8-6027BD558C36

Q33926696-062992D5-E519-4C6B-BD22-A53E8B0738AE

Q33926696-145E3B6D-1615-47D7-AD5C-3B9904E5A6CB

Q33926696-1FD0436E-AC0E-4523-91C0-1D0E36753727

Q33926696-20F5A473-94E1-4162-B579-851341E5D651

Q33926696-21A7FF10-37B3-4424-A077-BB247815F0BE

Q33926696-3C074347-99E5-4AA1-BC3A-B64A0769406F

Q33926696-44478B64-43DD-409F-9221-284C652179BD

Q33926696-44C3B90B-73DE-462A-92EA-6ADB5AB8AA21

Q33926696-57D8D21F-0325-4306-9D34-F1FFBB81AC57

P2888

Q33926696-335CC712-35EB-4173-A42C-EC7B50D06CE1

P304

Q33926696-0C5C51F7-236F-40B8-A4BC-8C3F00D8EAC0

P31

Q33926696-3B27B065-4519-4E57-9ACC-CC065B2CDBEE

P356

Q33926696-4284ECEB-E1F4-49DF-A3E3-AB91EAFC90E3

P433

Q33926696-80654744-FD51-46AC-A469-329A6517A9D5

P478

Q33926696-015D4347-DAA2-454F-A1D8-B47644C29EB2

P50

Q33926696-2002923F-3274-4279-BC95-200D82801D9C

Q33926696-BEBF4161-F4DC-4AF6-B07E-3482A390A53E

P577

Q33926696-E5803D82-D1B3-4B7B-A208-72C91469C209

P5875

Q33926696-07746AB2-AC4C-4BCD-B095-691EC71BC8AE

P6179

Q33926696-7A4F49C8-DF27-46ED-8118-E9F63EBD1329

P698

Q33926696-05CD87D9-D678-4802-854D-DF69E51CBB99

P921

Q33926696-21A80E38-71F1-4745-88D2-272DA21606B1

P932

Q33926696-5A2ABA54-FC9C-4367-8D48-6148BF349087

P356

S00439-011-1106-6

P1433

P1476

Increased prevalence of seizur ...... orbid autism spectrum disorder

@en

P2093

Danh V Nguyen

http://www.w3.org/2001/XMLSchema#string

David Hessl

http://www.w3.org/2001/XMLSchema#string

Flora Tassone

http://www.w3.org/2001/XMLSchema#string

Meredith Laird

http://www.w3.org/2001/XMLSchema#string

Randi J Hagerman

http://www.w3.org/2001/XMLSchema#string

Susan W Harris

http://www.w3.org/2001/XMLSchema#string

Weerasak Chonchaiya

http://www.w3.org/2001/XMLSchema#string

Yi Mu

http://www.w3.org/2001/XMLSchema#string

P2860

Advances in the treatment of fragile X syndrome

Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X

Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

The role of fragile X mental retardation protein in major mental disorders.

Fragile X: a family of disorders.

Broad clinical involvement in a family affected by the fragile X premutation.

Seizures in fragile X syndrome: characteristics and comorbid diagnoses.

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

Fragile X and autism: Intertwined at the molecular level leading to targeted treatments.

P2888

s00439-011-1106-6

P304

581-589

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1007/S00439-011-1106-6

http://www.w3.org/2001/XMLSchema#string

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

131

http://www.w3.org/2001/XMLSchema#string

P50

Andrea Schneider

P577

2011-10-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

51723763

http://www.w3.org/2001/XMLSchema#string

P6179

1029513592

http://www.w3.org/2001/XMLSchema#string

P698

22001913

http://www.w3.org/2001/XMLSchema#string

P921

Autism spectrum

P932

4105134

http://www.w3.org/2001/XMLSchema#string