histidine has been researched along with Developmental Disabilities in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (62.50) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Brinkmann, U; Hawer, H; Kung, A; Malhotra, A; Mayer, K; Mendelsohn, BA; Schaffrath, R; Schleit, J; Tuupanen, S | 1 |
| Fuchs, O; Pfarr, N; Pohlenz, J; Schmidt, H | 1 |
| Bax, R; Freisinger, P; Horn, N; Horváth, R; Jaksch, M; Mayr, JA; Merl, T; Moller, LB; Müller-Höcker, J; Pongratz, D; Rubio, R | 1 |
| Levy, HL; Scriver, CR | 1 |
| Coulombe, JT; Hirsch, BZ; Kammerer, BL; Levy, HL; Scriver, CR | 1 |
| Appleton, RE; Chitayat, D; Hall, JG; Jan, JE; Kennedy, R | 1 |
| Ishikawa, M | 1 |
| Bakwin, H | 1 |
1 review(s) available for histidine and Developmental Disabilities
| Article | Year |
|---|---|
Delayed speech. Developmental mutism.
Topics: Autistic Disorder; Brain Damage, Chronic; Child, Preschool; Developmental Disabilities; Diagnosis, Differential; Diseases in Twins; Emotions; Hearing Disorders; Histidine; Humans; Intellectual Disability; Mutism; Parent-Child Relations; Schizophrenia, Childhood; Speech Disorders; Verbal Behavior | 1968 |
7 other study(ies) available for histidine and Developmental Disabilities
| Article | Year |
|---|---|
Diphthamide-deficiency syndrome: a novel human developmental disorder and ribosomopathy.
Topics: Cell Line; Developmental Disabilities; Heart Defects, Congenital; Histidine; Humans; Infant; Loss of Function Mutation; Male; Megalencephaly; Proteins; Ribosomes; Saccharomyces cerevisiae; Syndrome | 2020 |
Elevated serum triiodothyronine and intellectual and motor disability with paroxysmal dyskinesia caused by a monocarboxylate transporter 8 gene mutation.
Topics: Arginine; Child; Chorea; Developmental Disabilities; DNA Mutational Analysis; Enzyme-Linked Immunosorbent Assay; Histidine; Humans; Intellectual Disability; Magnetic Resonance Imaging; Male; Monocarboxylic Acid Transporters; Mutation; Symporters; Triiodothyronine | 2009 |
Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolism.
Topics: Adenosine Triphosphatases; Blotting, Southern; Brain; Cataract; Cation Transport Proteins; Copper; Copper-Transporting ATPases; Cytochrome-c Oxidase Deficiency; Developmental Disabilities; DNA Mutational Analysis; Electrophysiology; Exons; Fibroblasts; Hearing Loss, Sensorineural; Histidine; Humans; Immunoblotting; Immunohistochemistry; Infant; Magnetic Resonance Imaging; Male; Mitochondria; Muscle Hypotonia; Muscle, Skeletal; Muscles; Mutation; Myoblasts; Recombinant Fusion Proteins; Superoxide Dismutase | 2005 |
Histidinaemia. Part I: Reconciling retrospective and prospective findings.
Topics: Amino Acid Metabolism, Inborn Errors; Central Nervous System Diseases; Child; Developmental Disabilities; Histidine; Humans; Infant, Newborn; Mass Screening; Phenotype; Prospective Studies; Retrospective Studies | 1983 |
Histidinaemia. Part III: Impact; a prospective study.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Developmental Disabilities; Female; Histidine; Humans; Intelligence Tests; Male; Phenotype; Prospective Studies | 1983 |
Joubert's syndrome associated with congenital ocular fibrosis and histidinemia.
Topics: Ataxia; Cerebellum; Developmental Disabilities; Female; Fibrosis; Histidine; Humans; Infant; Muscular Diseases; Oculomotor Muscles; Psychomotor Performance; Respiration Disorders; Syndrome; Tomography, X-Ray Computed | 1989 |
Developmental disorders in histidinemia--follow-up study of language development in histidinemia.
Topics: Child; Child, Preschool; Developmental Disabilities; Female; Follow-Up Studies; Histidine; Humans; Language Development; Male | 1987 |