Page last updated: 2024-08-17

methionine and Respiration Disorders

methionine has been researched along with Respiration Disorders in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Arne-Bes, MC; de Seze, J; Dubourg, O; Hache, JC; Stojkovic, T; Tardieu, S; Vermersch, P	1
ANTENER, I; HOOFT, C; OYAERT, W; SNOECK, J; TIMMERMANS, J; VANDENHENDE, C	1

Other Studies

2 other study(ies) available for methionine and Respiration Disorders

Article	Year
Autonomic and respiratory dysfunction in Charcot-Marie-Tooth disease due to Thr124Met mutation in the myelin protein zero gene. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2003, Volume: 114, Issue:9 Topics: Adult; Aged; Autonomic Nervous System Diseases; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; Evoked Potentials; Family Health; Female; France; Genetic Linkage; Humans; Male; Methionine; Middle Aged; Muscles; Myelin P0 Protein; Neural Conduction; Point Mutation; Polymerase Chain Reaction; Pupil; Respiration Disorders; Respiratory Tract Diseases; Threonine; Urinary Bladder	2003
METHIONINE MALABSORPTION IN A MENTALLY DEFECTIVE CHILD. Lancet (London, England), 1964, Jul-04, Volume: 2, Issue:7349 Topics: Amino Acid Metabolism, Inborn Errors; Child; Congenital Abnormalities; Diarrhea; Diarrhea, Infantile; Feces; Hair; Humans; Hydroxybutyrates; Intellectual Disability; Intestines; Methionine; Proteins; Respiration Disorders; Respiratory Tract Diseases; Seizures; Urine	1964

Article

Year

Autonomic and respiratory dysfunction in Charcot-Marie-Tooth disease due to Thr124Met mutation in the myelin protein zero gene.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2003, Volume: 114, Issue:9

Topics: Adult; Aged; Autonomic Nervous System Diseases; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; Evoked Potentials; Family Health; Female; France; Genetic Linkage; Humans; Male; Methionine; Middle Aged; Muscles; Myelin P0 Protein; Neural Conduction; Point Mutation; Polymerase Chain Reaction; Pupil; Respiration Disorders; Respiratory Tract Diseases; Threonine; Urinary Bladder

2003

METHIONINE MALABSORPTION IN A MENTALLY DEFECTIVE CHILD.

Lancet (London, England), 1964, Jul-04, Volume: 2, Issue:7349

Topics: Amino Acid Metabolism, Inborn Errors; Child; Congenital Abnormalities; Diarrhea; Diarrhea, Infantile; Feces; Hair; Humans; Hydroxybutyrates; Intellectual Disability; Intestines; Methionine; Proteins; Respiration Disorders; Respiratory Tract Diseases; Seizures; Urine

1964