Page last updated: 2024-08-17

lysine and External Ophthalmoplegia

lysine has been researched along with External Ophthalmoplegia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Andrews, C; Balasubramanian, R; Chan, WM; Chew, S; Engle, EC; Kang, PB; MacKinnon, SE	1
Brusco, A; Cagnoli, C; Di Bella, D; Di Donato, S; Gellera, C; Mariotti, C; Seri, M; Taroni, F	1

Other Studies

2 other study(ies) available for lysine and External Ophthalmoplegia

Article	Year
Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndrome. The Journal of clinical endocrinology and metabolism, 2015, Volume: 100, Issue:3 Topics: Adult; Aged; Amino Acid Substitution; Child; Child, Preschool; Developmental Disabilities; Endocrine System Diseases; Eye Diseases, Hereditary; Female; Fibrosis; Glutamic Acid; Humans; Kallmann Syndrome; Lysine; Male; Ophthalmoplegia; Pedigree; Phenotype; Syndrome; Tubulin	2015
Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. Cerebellum (London, England), 2008, Volume: 7, Issue:2 Topics: Adolescent; Adult; Aged; Base Sequence; Brain; Child; Chromosome Mapping; Chromosomes, Human, Pair 18; Female; Genes, Dominant; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Ophthalmoplegia; Pedigree; Phenotype; Point Mutation; Polymorphism, Single Nucleotide; Spinocerebellar Ataxias; Young Adult	2008

Article

Year

Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndrome.

The Journal of clinical endocrinology and metabolism, 2015, Volume: 100, Issue:3

Topics: Adult; Aged; Amino Acid Substitution; Child; Child, Preschool; Developmental Disabilities; Endocrine System Diseases; Eye Diseases, Hereditary; Female; Fibrosis; Glutamic Acid; Humans; Kallmann Syndrome; Lysine; Male; Ophthalmoplegia; Pedigree; Phenotype; Syndrome; Tubulin

2015

Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.

Cerebellum (London, England), 2008, Volume: 7, Issue:2

Topics: Adolescent; Adult; Aged; Base Sequence; Brain; Child; Chromosome Mapping; Chromosomes, Human, Pair 18; Female; Genes, Dominant; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Ophthalmoplegia; Pedigree; Phenotype; Point Mutation; Polymorphism, Single Nucleotide; Spinocerebellar Ataxias; Young Adult

2008