glutamine and Microcephaly

glutamine has been researched along with Microcephaly in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (33.33)	18.7374
1990's	1 (33.33)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (33.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
de Koning, TJ	1
Duc, G; Gitzelmann, R; Steinmann, B; Superti-Furga, A	1
Howell, RR; Stevenson, RE	1

Reviews

2 review(s) available for glutamine and Microcephaly

Article	Year
Amino acid synthesis deficiencies. Journal of inherited metabolic disease, 2017, Volume: 40, Issue:4 Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Asparagine; Brain Diseases; Central Nervous System; Fetal Growth Retardation; Glutamine; High-Throughput Nucleotide Sequencing; Humans; Ichthyosis; Limb Deformities, Congenital; Metabolic Diseases; Mice; Microcephaly; Proline; Serine	2017
The offspring of phenylketonuric women. Social biology, 1971, Volume: 18 Topics: Abortion, Spontaneous; Adult; Birth Weight; Black or African American; Brain Chemistry; Breast Feeding; Child, Preschool; Congenital Abnormalities; Diet Therapy; Female; Glutamine; Heart Auscultation; Heterozygote; Hexokinase; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Intelligence Tests; Male; Maryland; Microcephaly; Myelin Sheath; Nerve Tissue Proteins; Phenylacetates; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Prenatal Care; Pyruvate Kinase; Umbilical Cord	1971

Article

Year

Amino acid synthesis deficiencies.

Journal of inherited metabolic disease, 2017, Volume: 40, Issue:4

Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Asparagine; Brain Diseases; Central Nervous System; Fetal Growth Retardation; Glutamine; High-Throughput Nucleotide Sequencing; Humans; Ichthyosis; Limb Deformities, Congenital; Metabolic Diseases; Mice; Microcephaly; Proline; Serine

2017

The offspring of phenylketonuric women.

Social biology, 1971, Volume: 18

Topics: Abortion, Spontaneous; Adult; Birth Weight; Black or African American; Brain Chemistry; Breast Feeding; Child, Preschool; Congenital Abnormalities; Diet Therapy; Female; Glutamine; Heart Auscultation; Heterozygote; Hexokinase; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Intelligence Tests; Male; Maryland; Microcephaly; Myelin Sheath; Nerve Tissue Proteins; Phenylacetates; Phenylalanine; Phenylketonurias; Pregnancy; Pregnancy Complications; Prenatal Care; Pyruvate Kinase; Umbilical Cord

1971

Other Studies

1 other study(ies) available for glutamine and Microcephaly

Article	Year
Maternal phenylketonuria syndrome in cousins caused by mild, unrecognized phenylketonuria in their mothers homozygous for the phenylalanine hydroxylase Arg-261-Gln mutation. European journal of pediatrics, 1991, Volume: 150, Issue:7 Topics: Adult; Arginine; Base Sequence; Female; Glutamine; Homozygote; Humans; Infant; Infant, Newborn; Male; Microcephaly; Molecular Sequence Data; Mothers; Mutation; Pedigree; Phenylalanine Hydroxylase; Phenylketonurias	1991

Article

Year

Maternal phenylketonuria syndrome in cousins caused by mild, unrecognized phenylketonuria in their mothers homozygous for the phenylalanine hydroxylase Arg-261-Gln mutation.

European journal of pediatrics, 1991, Volume: 150, Issue:7

Topics: Adult; Arginine; Base Sequence; Female; Glutamine; Homozygote; Humans; Infant; Infant, Newborn; Male; Microcephaly; Molecular Sequence Data; Mothers; Mutation; Pedigree; Phenylalanine Hydroxylase; Phenylketonurias

1991