Page last updated: 2024-10-16

ammonium hydroxide and Ataxia

ammonium hydroxide has been researched along with Ataxia in 12 studies

azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.

Ataxia: Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions.

Research Excerpts

ExcerptRelevanceReference
"Ataxia has been suggested in the literature to be a symptom of hepatic encephalopathy (HE), but so far has not been objectively quantified."1.35Postural control in patients with liver cirrhosis: a posturographic study. ( Fialka-Moser, V; Gangl, A; Mittermaier, C; Peck-Radosavljevic, M; Schmid, M; Voller, B, 2009)
"Late-onset OTC deficiency has been described in patients of all ages."1.29Vomiting, ataxia, and altered mental status in an adolescent: late-onset ornithine transcarbamylase deficiency. ( Myers, JH; Shook, JE, 1996)
"Rett syndrome was also observed in two sisters."1.27The clinical pattern of the Rett syndrome. ( Hanefeld, F, 1985)

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19908 (66.67)18.7374
1990's2 (16.67)18.2507
2000's2 (16.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Schmid, M1
Mittermaier, C1
Voller, B1
Fialka-Moser, V1
Gangl, A1
Peck-Radosavljevic, M1
Kim, JM1
Ryu, WS1
Hwang, YH1
Kim, JS1
Hagberg, B1
Aicardi, J1
Dias, K1
Ramos, O1
Nagura, H1
Yamanouchi, H1
Myers, JH1
Shook, JE1
Harendra de Silva, DG1
Rowe, PC1
Newman, SL1
Brusilow, SW1
Hanefeld, F1
Potter, JL1
Timmons, GD1
West, R1
Silvidi, AA1
Brenton, DP1
Cusworth, DC1
Hartley, S1
Lumley, S1
Kuzemko, JA1
Wright, T1
Pollitt, R1
Shih, VE1
Efron, ML1
Moser, HW1

Clinical Trials (3)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Rett Syndrome, MECP2 Duplication Disorder, and Rett- Related Disorders Natural History Protocol[NCT02738281]1,044 participants (Actual)Observational2015-11-30Completed
Biobanking of Rett Syndrome and Related Disorders Protocol[NCT02705677]752 participants (Actual)Observational2017-09-01Completed
Investigation on the Effects of an Osteopathic Manipulative Treatment for Constipation in People With Rett Syndrome[NCT05687214]12 participants (Actual)Interventional2022-11-16Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Other Studies

12 other studies available for ammonium hydroxide and Ataxia

ArticleYear
Postural control in patients with liver cirrhosis: a posturographic study.
    European journal of gastroenterology & hepatology, 2009, Volume: 21, Issue:8

    Topics: Adult; Aged; Aged, 80 and over; Ammonia; Ataxia; Case-Control Studies; Female; Hepatic Encephalopath

2009
Aggravation of ataxia due to acetazolamide induced hyperammonaemia in episodic ataxia.
    Journal of neurology, neurosurgery, and psychiatry, 2007, Volume: 78, Issue:7

    Topics: Acetazolamide; Acidosis; Ammonia; Ataxia; Carbonic Anhydrase Inhibitors; Disease Progression; Humans

2007
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.
    Annals of neurology, 1983, Volume: 14, Issue:4

    Topics: Adolescent; Adult; Ammonia; Apraxias; Ataxia; Autistic Disorder; Child; Child Development; Child, Pr

1983
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.
    Annals of neurology, 1983, Volume: 14, Issue:4

    Topics: Adolescent; Adult; Ammonia; Apraxias; Ataxia; Autistic Disorder; Child; Child Development; Child, Pr

1983
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.
    Annals of neurology, 1983, Volume: 14, Issue:4

    Topics: Adolescent; Adult; Ammonia; Apraxias; Ataxia; Autistic Disorder; Child; Child Development; Child, Pr

1983
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.
    Annals of neurology, 1983, Volume: 14, Issue:4

    Topics: Adolescent; Adult; Ammonia; Apraxias; Ataxia; Autistic Disorder; Child; Child Development; Child, Pr

1983
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.
    Annals of neurology, 1983, Volume: 14, Issue:4

    Topics: Adolescent; Adult; Ammonia; Apraxias; Ataxia; Autistic Disorder; Child; Child Development; Child, Pr

1983
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.
    Annals of neurology, 1983, Volume: 14, Issue:4

    Topics: Adolescent; Adult; Ammonia; Apraxias; Ataxia; Autistic Disorder; Child; Child Development; Child, Pr

1983
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.
    Annals of neurology, 1983, Volume: 14, Issue:4

    Topics: Adolescent; Adult; Ammonia; Apraxias; Ataxia; Autistic Disorder; Child; Child Development; Child, Pr

1983
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.
    Annals of neurology, 1983, Volume: 14, Issue:4

    Topics: Adolescent; Adult; Ammonia; Apraxias; Ataxia; Autistic Disorder; Child; Child Development; Child, Pr

1983
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.
    Annals of neurology, 1983, Volume: 14, Issue:4

    Topics: Adolescent; Adult; Ammonia; Apraxias; Ataxia; Autistic Disorder; Child; Child Development; Child, Pr

1983
[A case of portal-systemic shunt with progressive ataxia].
    Rinsho shinkeigaku = Clinical neurology, 1993, Volume: 33, Issue:3

    Topics: Aged; Ammonia; Ataxia; Hepatic Encephalopathy; Humans; Male; Portal Vein

1993
Vomiting, ataxia, and altered mental status in an adolescent: late-onset ornithine transcarbamylase deficiency.
    The American journal of emergency medicine, 1996, Volume: 14, Issue:6

    Topics: Adolescent; Age of Onset; Amino Acid Metabolism, Inborn Errors; Ammonia; Ataxia; Cognition Disorders

1996
Rett syndrome in Sri Lanka.
    The Ceylon medical journal, 1988, Volume: 33, Issue:2

    Topics: Ammonia; Ataxia; Autistic Disorder; Child; Dementia; Female; Functional Laterality; Humans; Seizures

1988
Natural history of symptomatic partial ornithine transcarbamylase deficiency.
    The New England journal of medicine, 1986, Feb-27, Volume: 314, Issue:9

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Ataxia; Child, Preschool; Coma; Diagnosis, Differenti

1986
The clinical pattern of the Rett syndrome.
    Brain & development, 1985, Volume: 7, Issue:3

    Topics: Adolescent; Adult; Ammonia; Ataxia; Child; Child Development; Child, Preschool; Dementia; Female; Fo

1985
Arginosuccinicaciduria. The hair abnormality.
    American journal of diseases of children (1960), 1974, Volume: 127, Issue:5

    Topics: Amino Acids; Ammonia; Arginine; Ataxia; Blood Urea Nitrogen; Child, Preschool; Chromatography, Paper

1974
Argininosuccinicaciduria: clinical, metabolic and dietary study.
    Journal of mental deficiency research, 1974, Volume: 18, Issue:0

    Topics: Affective Symptoms; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginase; Arginine; Ataxia; Child

1974
Psychomotor retardation, epileptic and stuporous attacks, irritability and ataxia associated with ammonia intoxication, high blood ornithine levels and increased homocitruline in the urine.
    Proceedings of the Royal Society of Medicine, 1973, Volume: 66, Issue:3

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Ataxia; Citrulline; Epilepsy; Female; Humans;

1973
Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.
    American journal of diseases of children (1960), 1969, Volume: 117, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Ataxia; Child, Preschool; Citrulline; Di

1969