threonine and Child Development Deviations

threonine has been researched along with Child Development Deviations 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
Dockter, G; Gomes, TS; Gortner, L; Leitner, D; Rohrer, T; Thakker, RV	1
Robertson, SP	1

Other Studies

2 other study(ies) available for threonine and Child Development Deviations

Article	Year
HDR syndrome: a follow-up genotype-phenotype analysis of a de novo missense Thr272Ile mutation in exon 4 of GATA3. Klinische Padiatrie, 2012, Volume: 224, Issue:7 Topics: Child; Child, Preschool; Combined Modality Therapy; Developmental Disabilities; DNA Mutational Analysis; Exons; Follow-Up Studies; GATA3 Transcription Factor; Genetic Carrier Screening; Genotype; Hearing Loss, Sensorineural; Humans; Hypoparathyroidism; Infant; Isoleucine; Male; Mutation, Missense; Nephrosis; Phenotype; Threonine	2012
Filamin a, periventricular nodular heterotopia, and West syndrome. Epilepsia, 2006, Volume: 47, Issue:6 Topics: Brain Diseases; Cerebral Ventricles; Choristoma; Contractile Proteins; Developmental Disabilities; Electroencephalography; Exons; Female; Filamins; Genetic Diseases, X-Linked; Humans; Infant; Male; Methionine; Microfilament Proteins; Mutation; Mutation, Missense; Pedigree; Phenotype; Polymorphism, Single Nucleotide; Sequence Analysis, Protein; Spasms, Infantile; Threonine	2006

Article

Year

HDR syndrome: a follow-up genotype-phenotype analysis of a de novo missense Thr272Ile mutation in exon 4 of GATA3.

Klinische Padiatrie, 2012, Volume: 224, Issue:7

Topics: Child; Child, Preschool; Combined Modality Therapy; Developmental Disabilities; DNA Mutational Analysis; Exons; Follow-Up Studies; GATA3 Transcription Factor; Genetic Carrier Screening; Genotype; Hearing Loss, Sensorineural; Humans; Hypoparathyroidism; Infant; Isoleucine; Male; Mutation, Missense; Nephrosis; Phenotype; Threonine

2012

Filamin a, periventricular nodular heterotopia, and West syndrome.

Epilepsia, 2006, Volume: 47, Issue:6

Topics: Brain Diseases; Cerebral Ventricles; Choristoma; Contractile Proteins; Developmental Disabilities; Electroencephalography; Exons; Female; Filamins; Genetic Diseases, X-Linked; Humans; Infant; Male; Methionine; Microfilament Proteins; Mutation; Mutation, Missense; Pedigree; Phenotype; Polymorphism, Single Nucleotide; Sequence Analysis, Protein; Spasms, Infantile; Threonine

2006