glutamine has been researched along with Syndrome in 25 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (24.00) | 18.7374 |
| 1990's | 4 (16.00) | 18.2507 |
| 2000's | 10 (40.00) | 29.6817 |
| 2010's | 4 (16.00) | 24.3611 |
| 2020's | 1 (4.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ding, Q; Liang, M | 1 |
| Hirai, N; Moriyama, Y; Takanashi, JI; Yasukawa, K; Yoshimaru, D | 1 |
| Abudu, H; Ahemaiti, A; Aximujiang, K; Wu, G; Yunusi, K; Zhang, J | 1 |
| Accorsi, P; Bernardina, BD; Bettella, E; Darra, F; Galli, J; Giordano, L; Marchi, M; Murgia, A; Russo, S; Sartori, S; Tiberti, A; Vignoli, A | 1 |
| Czerwinski, M; Duk, M; Grodecka, M; Jaskiewicz, E; Kaczmarek, R; Laskowska, A; Lisowska, E; Lukasiewicz, J; Majorczyk, E; Smolarek, D; Suchanowska, A; Wasniowska, K | 1 |
| Del Castillo, I; Menéndez, I; Migliosi, V; Modamio-Høybjør, S; Moreno, F; Moreno-Pelayo, MA; Rodríguez-Ballesteros, M; Tellería, D; Villamar, M | 1 |
| Chantry, A; Farrell, ER; Munsterberg, A; Smith, T; Sweetman, D | 1 |
| GLOBUS, M; MCCOLL, JD; ROBINSON, S | 1 |
| Gekka, T; Hayashi, T; Kitahara, K; Kozaki, K; Kubo, A; Nakamura, Y; Omoto, S; Takeuchi, T; Toda, K; Watanabe, A | 1 |
| Traboulsi, EI | 1 |
| Hadzsiev, K; Kellermayer, R; Kestilä, M; Kosztolányi, G; Siitonen, HA | 1 |
| Adès, LC; Gilmour, E; Graf, N; Holme, SA; Maclean, K; Moss, C; Onikul, E; Scheffer, H; Smith, GH; Taylor, M; van Bokhoven, H | 1 |
| Balduini, CL; De Candia, E; Savoia, A | 1 |
| Blanke, CD; Chan, JS; Harding, CO | 1 |
| Nicklas, WJ | 1 |
| Khaĭlova, IM; Khokhlov, AP; Mel'nichuk, PV | 1 |
| Krivopusk, ME | 1 |
| Bartolone, L; Benvenga, S; Filetti, S; Pontecorvi, A; Regalbuto, C; Trimarchi, F | 1 |
| Mori, N; Oishi, M; Osaka, S; Sawada, S; Takasu, T; Uchiyama, T; Yamamoto, M | 1 |
| Komori, S; Koyama, K; Sakata, K; Shima, H; Tanaka, H | 1 |
| Chang, JG; Lee, CC; Tsai, FJ; Wu, JY; Yang, CF | 1 |
| Lazareva, EB; Men'shikov, DD; Narodetskaia, RV; Popova, TS; Poriadkov, LF; Shramko, LU; Tropskaia, NS | 1 |
| Knopman, DS; Shih, VE; Tuchman, M | 1 |
| Max, SR; Silbergeld, EK | 1 |
| Ionasescu, V; Mueller, S; Stegink, L; Weinstein, M | 1 |
2 review(s) available for glutamine and Syndrome
| Article | Year |
|---|---|
Amino acid metabolism in the central nervous system: role of glutamate dehydrogenase.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Central Nervous System; Cerebellar Ataxia; Enzyme Activation; gamma-Aminobutyric Acid; Glutamate Dehydrogenase; Glutamate Synthase; Glutamates; Glutamic Acid; Glutamine; Humans; Leucine; Mitochondria; NADP; Nerve Endings; Neuroglia; Rats; Syndrome | 1984 |
[Nutritional agents and probiotics in the treatment of intestinal insufficiency syndrome and normalization of intestinal microbiocenosis].
Topics: Arginine; Fatty Acids; Gastrointestinal Diseases; Glutamine; Humans; Nutritional Status; Pectins; Syndrome | 2001 |
23 other study(ies) available for glutamine and Syndrome
| Article | Year |
|---|---|
Arg1201Gln mutation of insulin receptor impairs tyrosine kinase activity and causes insulin resistance: a case report.
Topics: Adolescent; Amino Acid Substitution; Antigens, CD; Arginine; China; Female; Glutamine; Heterozygote; Humans; Hyperandrogenism; Insulin Resistance; Metabolic Syndrome; Mutation, Missense; Protein-Tyrosine Kinases; Receptor, Insulin; Syndrome | 2020 |
A new infectious encephalopathy syndrome, clinically mild encephalopathy associated with excitotoxicity (MEEX).
Topics: Brain; Brain Diseases; Child, Preschool; Consciousness Disorders; Diffusion Magnetic Resonance Imaging; Follow-Up Studies; Glutamic Acid; Glutamine; Humans; Infant; Magnetic Resonance Spectroscopy; Male; Retrospective Studies; Syndrome | 2017 |
[Metabonomic analysis of the urine from rat model with abnormal sapra syndrome].
Topics: Amino Acids; Animals; Citric Acid; Creatine; Disease Models, Animal; Energy Metabolism; Glutamine; Glycoproteins; Isoleucine; Leucine; Metabolomics; Phenylalanine; Rats; Rats, Wistar; Syndrome | 2017 |
Familial Ohtahara syndrome due to a novel ARX gene mutation.
Topics: Base Sequence; Epilepsy; Exons; Family; Female; Genes, Homeobox; Glutamine; Homeodomain Proteins; Humans; Infant, Newborn; Male; Mutation; Pedigree; Phenotype; Spasms, Infantile; Syndrome; Transcription Factors | 2010 |
A single point mutation in the gene encoding Gb3/CD77 synthase causes a rare inherited polyagglutination syndrome.
Topics: Amino Acid Substitution; Carbohydrate Sequence; Cell Line, Tumor; Embryonal Carcinoma Stem Cells; Flow Cytometry; Galactosyltransferases; Genetic Predisposition to Disease; Genotype; Globosides; Glutamic Acid; Glutamine; Hemagglutination; Humans; Molecular Sequence Data; Phenotype; Point Mutation; Polymorphism, Single Nucleotide; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Syndrome | 2012 |
Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss.
Topics: Amino Acid Sequence; Amino Acid Substitution; Female; Gene Frequency; Genetic Markers; Glutamine; Hearing Loss, Sensorineural; Humans; Male; Membrane Proteins; Molecular Sequence Data; Mutation; Nuclear Family; Pedigree; Spain; Syndrome | 2002 |
The conserved glutamine-rich region of chick csal1 and csal3 mediates protein interactions with other spalt family members. Implications for Townes-Brocks syndrome.
Topics: Amino Acid Sequence; Animals; Cell Line; Chick Embryo; Conserved Sequence; Disease Models, Animal; Extremities; Glutamine; Homeodomain Proteins; Humans; Molecular Sequence Data; Morphogenesis; Peptide Fragments; Protein Isoforms; Recombinant Proteins; Syndrome; Transcription Factors; Transfection; Xenopus Proteins; Zinc Fingers | 2003 |
AN ATTEMPTED REVERSAL OF THALIDOMIDE EMBRYOPATHY IN THE RAT BY GLUTAMINE.
Topics: Abnormalities, Drug-Induced; Fetal Diseases; Glutamates; Glutamine; Pathology; Pharmacology; Pregnancy; Pregnancy, Animal; Rats; Research; Syndrome; Thalidomide; Toxicology | 1965 |
Enhanced S-cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X).
Topics: Adolescent; Asian People; Base Sequence; Codon, Nonsense; Codon, Terminator; Color Vision Defects; Electroretinography; Fundus Oculi; Glutamine; Humans; Male; Night Blindness; Orphan Nuclear Receptors; Pedigree; Receptors, Cytoplasmic and Nuclear; Retinal Cone Photoreceptor Cells; Retinal Diseases; Syndrome; Transcription Factors; Visual Acuity | 2004 |
Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements.
Topics: Adenine; Adolescent; Adult; Amino Acid Substitution; Arginine; Child; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 11; Cranial Nerves; Female; Fibrosis; Genes, Recessive; Genetic Variation; Glutamine; Guanine; Humans; Kinesins; Male; Mobius Syndrome; Mutation; Nerve Tissue Proteins; Oculomotor Muscles; Ophthalmoplegia; Pedigree; Phenotype; Scoliosis; Syndrome | 2004 |
A patient with Rothmund-Thomson syndrome and all features of RAPADILINO.
Topics: Abnormalities, Multiple; Adenosine Triphosphatases; Amino Acid Substitution; Arginine; Bone and Bones; Child; Cytosine; Diarrhea; DNA Helicases; Glutamine; Growth Disorders; Guanine; Humans; Joint Dislocations; Limb Deformities, Congenital; Male; Mutation; Mutation, Missense; Palate; Patella; Radius; RecQ Helicases; Rothmund-Thomson Syndrome; Syndrome; Thymine | 2005 |
EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype-phenotype correlation?
Topics: Abnormalities, Multiple; Adult; Arginine; Child, Preschool; Cleft Lip; Cleft Palate; DNA-Binding Proteins; Ectodermal Dysplasia; Female; Fingers; Genotype; Glutamine; Humans; Infant; Male; Middle Aged; Pedigree; Phenotype; Point Mutation; Syndrome; Trans-Activators; Transcription Factors; Tumor Suppressor Proteins; Urination Disorders | 2007 |
Why the disorder induced by GATA1 Arg216Gln mutation should be called "X-linked thrombocytopenia with thalassemia" rather than "X-linked gray platelet syndrome".
Topics: Arginine; Blood Platelets; GATA1 Transcription Factor; Genes, X-Linked; Glutamine; Humans; Mutation; Syndrome; Terminology as Topic; Thalassemia; Thrombocytopenia | 2007 |
Postchemotherapy hyperammonemic encephalopathy emulating ornithine transcarbamoylase (OTC) deficiency.
Topics: Adult; Arginine; Carcinoma, Hepatocellular; Citrulline; Female; Glutamine; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver Neoplasms; Ornithine; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Polymorphism, Single-Stranded Conformational; Syndrome | 2008 |
[Early diagnosis of the Tourette syndrome].
Topics: Adolescent; Child; Female; Glutamine; Haloperidol; Humans; Male; Neurasthenia; Phenylacetates; Syndrome; Thioridazine; Tourette Syndrome | 1980 |
[Amino acid composition of cerebrospinal fluid in the epilepsy syndrome].
Topics: Amino Acids; Arachnoiditis; Brain Neoplasms; Chronic Disease; Encephalitis; Epilepsy; Glutamates; Glutamine; Humans; Syndrome | 1980 |
Three new mutations of thyroid hormone receptor-beta associated with resistance to thyroid hormone.
Topics: Adolescent; Adult; Amino Acid Sequence; Asparagine; Aspartic Acid; Base Sequence; Drug Resistance; Female; Glutamates; Glutamic Acid; Glutamine; Humans; Lysine; Male; Molecular Sequence Data; Point Mutation; Receptors, Thyroid Hormone; Sicily; Syndrome; Thyroid Hormones | 1994 |
Nasu-Hakola disease. A case accompanied by abnormalities in fatty acid composition of serum total lipids and amino acid analysis.
Topics: Adult; Amino Acids; Biopsy; Brain; Dementia; Fatty Acids; Glutamine; Humans; Lipids; Lipodystrophy; Male; Syndrome; Tomography, X-Ray Computed | 1993 |
DNA analysis of the androgen receptor gene in two cases with complete androgen insensitivity syndrome.
Topics: Adult; Binding Sites; Disorders of Sex Development; DNA; DNA Mutational Analysis; Gene Deletion; Genetic Linkage; Glutamine; Humans; Male; Point Mutation; Polymerase Chain Reaction; Receptors, Androgen; Sequence Analysis, DNA; Syndrome; X Chromosome | 1997 |
A novel mutation (Q239R) identified in a Taiwan Chinese patient with type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome).
Topics: Alleles; Amino Acid Substitution; Arginine; Asian People; China; Genes, Recessive; Germ-Line Mutation; Glutamine; Humans; Mucopolysaccharidosis VI; Mutation, Missense; N-Acetylgalactosamine-4-Sulfatase; Syndrome; Taiwan | 2000 |
Episodic hyperammonemia in adult siblings with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome.
Topics: Adult; Ammonia; Citrulline; Female; Fibroblasts; Glutamine; Humans; Leucine; Male; Metabolism, Inborn Errors; Ornithine; Phenylbutyrates; Recurrence; Syndrome; Urea | 1990 |
Skeletal muscle glucocorticoid receptor and glutamine synthetase activity in the wasting syndrome in rats treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin.
Topics: Animals; Body Weight; Dioxins; Glutamate-Ammonia Ligase; Glutamine; Male; Muscles; Polychlorinated Dibenzodioxins; Rats; Rats, Inbred F344; Receptors, Glucocorticoid; Syndrome | 1987 |
Amino acid abnormality in Sjögren-Larsson syndrome.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Dental Enamel Hypoplasia; Epilepsy; Ethylamines; Glutamine; Glycine; Histidine; Humans; Ichthyosis; Intellectual Disability; Isoleucine; Leucine; Lysine; Male; Muscle Spasticity; Retinal Degeneration; Serine; Syndrome; Valine | 1973 |