Page last updated: 2024-08-23

fomesafen and Genetic Diseases, X-Chromosome Linked

fomesafen has been researched along with Genetic Diseases, X-Chromosome Linked in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Al-Hamdani, S; Bregnhøj, J; Larsen, M; Sander, B; Schatz, P1
Ansaldo, AI; Benfenati, F; Cossette, P; Gravel, M; Nguyen, DK; Rouleau, I; Sénéchal, G1
PAINE, RS1

Other Studies

3 other study(ies) available for fomesafen and Genetic Diseases, X-Chromosome Linked

ArticleYear
Reappearance of the tapetal-like reflex after prolonged dark adaptation in a female carrier of RPGR ORF15 X-linked retinitis pigmentosa.
    Molecular vision, 2014, Volume: 20

    Topics: Child; Dark Adaptation; Electroretinography; Eye Proteins; Family; Female; Fundus Oculi; Genetic Diseases, X-Linked; Heterozygote; Humans; Male; Open Reading Frames; Pedigree; Reflex; Retinitis Pigmentosa; Tomography, Optical Coherence; Young Adult

2014
X-linked focal epilepsy with reflex bathing seizures: Characterization of a distinct epileptic syndrome.
    Epilepsia, 2015, Volume: 56, Issue:7

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Baths; Child; Epilepsies, Partial; Female; Genetic Diseases, X-Linked; Humans; Male; Middle Aged; Pedigree; Quebec; Reflex; Seizures; Syndrome

2015
THE EVOLUTION OF INFANTILE POSTURAL REFLEXES IN THE PRESENCE OF CHRONIC BRAIN SYNDROMES.
    Developmental medicine and child neurology, 1964, Volume: 6

    Topics: Ataxia; Athetosis; Brain; Cerebral Palsy; Child; Congenital Abnormalities; Dystonia Musculorum Deformans; Dystonic Disorders; Genetic Diseases, X-Linked; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Kernicterus; Movement Disorders; Muscle Spasticity; Paralysis; Posture; Reflex; Reflex, Abnormal; Syndrome

1964