alanine has been researched along with Syndrome in 44 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Orbofiban, despite no significant excess risk of ICH, was not effective in preventing ischemic stroke or TIA." | 9.12 | Risk factors for stroke after acute coronary syndromes in the Orbofiban in Patients with Unstable Coronary Syndromes--Thrombolysis In Myocardial Infarction (OPUS-TIMI) 16 study. ( Cannon, CP; Feske, SK; Murphy, S; Schwamm, LH; Smith, EE, 2006) |
| "Impairment of urea cycle function in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome is presumably caused, in some patients, by deficient transport of ornithine from cytoplasm into mitochondria." | 7.67 | Ornithine loading did not prevent induced hyperammonemia in a patient with hyperornithinemia-hyperammonemia-homocitrullinuria syndrome. ( Clow, CL; Mackenzie, S; Scriver, CR; Simell, O, 1985) |
| "A case of glucagonoma syndrome with necrolytic migratory erythema, glossitis, anemia, hyperglucagonemia and a malignant, pancreatic A-cell tumour in a 68-year-old male is described." | 7.66 | Metabolic studies and glucagon gel filtration pattern before and after surgery in a case of glucagonoma syndrome. ( Berg, J; Bojs, G; Dymling, JF; Hallengren, B; Ljungberg, O; Thorell, JI; Tibblin, S; von Schenck, H, 1979) |
| "Reifenstein syndrome is an eponymic term that describes partial androgen-insensitive disorders." | 5.29 | A mutant androgen receptor from patients with Reifenstein syndrome: identification of the function of a conserved alanine residue in the D box of steroid receptors. ( Cato, AC; Denninger, A; Kaspar, F; Klocker, H, 1993) |
| " Orbofiban, despite no significant excess risk of ICH, was not effective in preventing ischemic stroke or TIA." | 5.12 | Risk factors for stroke after acute coronary syndromes in the Orbofiban in Patients with Unstable Coronary Syndromes--Thrombolysis In Myocardial Infarction (OPUS-TIMI) 16 study. ( Cannon, CP; Feske, SK; Murphy, S; Schwamm, LH; Smith, EE, 2006) |
| "A single exchange of an alanine to a threonine at amino acid position 596 in the androgen receptor has been identified as an inheritable trait in patients with Reifenstein syndrome." | 3.69 | A single amino acid exchange abolishes dimerization of the androgen receptor and causes Reifenstein syndrome. ( Cato, AC; Gast, A; Klocker, H; Neuschmid-Kaspar, F, 1995) |
| "Toxic Oil Syndrome is a multisystemic disease that occurred in epidemic proportions in Spain in 1981 caused by the ingestion of rapeseed oil denatured with aniline." | 3.69 | Study of apoptosis in human lymphocytes by toxic substances implicated in toxic oil syndrome. ( Cárdaba, B; Cortegano, I; de Andrés, B; del Pozo, V; Gallardo, S; Jurado, A; Lahoz, C; Palomino, P; Tramón, P, 1997) |
| "Impairment of urea cycle function in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome is presumably caused, in some patients, by deficient transport of ornithine from cytoplasm into mitochondria." | 3.67 | Ornithine loading did not prevent induced hyperammonemia in a patient with hyperornithinemia-hyperammonemia-homocitrullinuria syndrome. ( Clow, CL; Mackenzie, S; Scriver, CR; Simell, O, 1985) |
| "A case of glucagonoma syndrome with necrolytic migratory erythema, glossitis, anemia, hyperglucagonemia and a malignant, pancreatic A-cell tumour in a 68-year-old male is described." | 3.66 | Metabolic studies and glucagon gel filtration pattern before and after surgery in a case of glucagonoma syndrome. ( Berg, J; Bojs, G; Dymling, JF; Hallengren, B; Ljungberg, O; Thorell, JI; Tibblin, S; von Schenck, H, 1979) |
| "The MELAS has been related to mutation A3243G in most cases, but some other mitochondrial DNA mutations were described in the background of this syndrome as well." | 1.37 | A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome. ( Gál, A; Lukács, T; Molnár, MJ; Reményi, V; Semjén, J; Valikovics, A; Vastagh, I, 2011) |
| "The Timothy syndrome is a multisystem disorder associated with the mutation of a Gly residue (G402 or G406) in the Ca(v)1." | 1.35 | Introduction into Ca(v)2.1 of the homologous mutation of Ca(v)1.2 causing the Timothy syndrome questions the role of V421 in the phenotypic definition of P-type Ca(2+) channel. ( Cens, T; Charnet, P; Leyris, JP, 2008) |
| "In the family with syndactyly type V, we identified a missense mutation in the HOXD13 homeodomain, c." | 1.34 | Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome. ( Amzel, LM; Ao, Y; Jabs, EW; Leyva, JA; Liu, G; Liu, Q; Lo, WH; Shan, X; Sun, M; Yang, W; Zeng, X; Zhang, X; Zhao, J; Zhao, X; Zhu, H, 2007) |
| "Char syndrome is an autosomal dominant trait characterized by patent ductus arteriosus, facial dysmorphism and hand anomalies." | 1.31 | Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus. ( Burn, J; Davidson, HR; Diaz, GA; Gelb, BD; Goodship, J; Pierpont, ME; Satoda, M; Zhao, F, 2000) |
| " Oral GP IIb/IIIa inhibitors have been associated with an increased incidence of bleeding, but additional experience may permit the design of dosing regimens that decrease this risk." | 1.31 | Learning from the recently completed oral glycoprotein IIb/IIIa receptor antagonist trials. ( Cannon, CP, 2000) |
| "Reifenstein syndrome is an eponymic term that describes partial androgen-insensitive disorders." | 1.29 | A mutant androgen receptor from patients with Reifenstein syndrome: identification of the function of a conserved alanine residue in the D box of steroid receptors. ( Cato, AC; Denninger, A; Kaspar, F; Klocker, H, 1993) |
| "Thiamine treatment was followed by a decrease of serum alanine and blood pyruvate and lactate, but there was no clinical improvement during a period of 17 months." | 1.25 | Subacute necrotizing encephalomyelopathy. Clinical, ultrastructural, biochemical and therapeutic studies in an infant. ( Bassewitz, DB; Dominick, HC; Gröbe, H; Pfeiffer, RA, 1975) |
| "Orotic aciduria was present (max: 693 mg/day) and was related to NH4 levels." | 1.25 | [Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)]. ( Beaudry, MA; Collu, R; Dallairf, L; Ducharme, JR; Leboeuf, G; Letarte, J; Melancon, SB, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 15 (34.09) | 18.7374 |
| 1990's | 6 (13.64) | 18.2507 |
| 2000's | 17 (38.64) | 29.6817 |
| 2010's | 6 (13.64) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Khan, F | 1 |
| Parikh, MP | 1 |
| McCullough, AJ | 1 |
| McAninch, EA | 1 |
| Jo, S | 1 |
| Preite, NZ | 1 |
| Farkas, E | 1 |
| Mohácsik, P | 1 |
| Fekete, C | 1 |
| Egri, P | 1 |
| Gereben, B | 1 |
| Li, Y | 1 |
| Deng, Y | 1 |
| Patti, ME | 1 |
| Zevenbergen, C | 1 |
| Peeters, RP | 1 |
| Mash, DC | 1 |
| Bianco, AC | 1 |
| Cherkaoui Jaouad, I | 1 |
| El Alloussi, M | 1 |
| Chafai El Alaoui, S | 1 |
| Laarabi, FZ | 1 |
| Lyahyai, J | 1 |
| Sefiani, A | 1 |
| Cens, T | 1 |
| Leyris, JP | 1 |
| Charnet, P | 1 |
| Paranaíba, LM | 1 |
| Martelli-Júnior, H | 1 |
| Oliveira Swerts, MS | 1 |
| Line, SR | 1 |
| Coletta, RD | 1 |
| Parodi, S | 1 |
| Vollono, C | 1 |
| Baglietto, MP | 1 |
| Balestri, M | 1 |
| Di Duca, M | 1 |
| Landri, PA | 1 |
| Ceccherini, I | 1 |
| Ottonello, G | 1 |
| Cilio, MR | 1 |
| Vastagh, I | 1 |
| Gál, A | 1 |
| Reményi, V | 1 |
| Semjén, J | 1 |
| Lukács, T | 1 |
| Valikovics, A | 1 |
| Molnár, MJ | 1 |
| Itoh, S | 1 |
| Matsuoka, H | 1 |
| Yasuda, Y | 1 |
| Miyake, N | 1 |
| Suzuki, K | 1 |
| Yorifuji, T | 1 |
| Sugihara, S | 1 |
| Morrow, DA | 2 |
| Rifai, N | 2 |
| Sabatine, MS | 3 |
| Ayanian, S | 1 |
| Murphy, SA | 2 |
| de Lemos, JA | 2 |
| Braunwald, E | 2 |
| Cannon, CP | 6 |
| Reinders, J | 1 |
| Rozemuller, EH | 1 |
| Ongkosuwito, JV | 1 |
| Jager, MJ | 1 |
| Tilanus, MG | 1 |
| Suttorp-Schulten, MS | 1 |
| Kim, Y | 1 |
| Park, JY | 1 |
| Lee, TJ | 1 |
| Yoo, HW | 1 |
| DI SIMONE, A | 1 |
| FERRANTE, G | 1 |
| Kovar, D | 1 |
| Bentley, JH | 1 |
| Charlesworth, A | 1 |
| Rogers, WJ | 1 |
| Smith, EE | 1 |
| Murphy, S | 2 |
| Feske, SK | 1 |
| Schwamm, LH | 1 |
| Atar, S | 1 |
| Rosanio, S | 1 |
| Uretsky, BF | 1 |
| Birnbaum, Y | 1 |
| Stanley, CA | 1 |
| Zhao, X | 1 |
| Sun, M | 1 |
| Zhao, J | 1 |
| Leyva, JA | 1 |
| Zhu, H | 1 |
| Yang, W | 1 |
| Zeng, X | 1 |
| Ao, Y | 1 |
| Liu, Q | 1 |
| Liu, G | 1 |
| Lo, WH | 1 |
| Jabs, EW | 1 |
| Amzel, LM | 1 |
| Shan, X | 1 |
| Zhang, X | 1 |
| Fuse, N | 1 |
| Takahashi, K | 1 |
| Yokokura, S | 1 |
| Nishida, K | 1 |
| Scirica, BM | 1 |
| Wiviott, SD | 1 |
| McCabe, CH | 1 |
| Lew, ED | 1 |
| Bae, JH | 1 |
| Rohmann, E | 1 |
| Wollnik, B | 1 |
| Schlessinger, J | 1 |
| Gast, A | 1 |
| Neuschmid-Kaspar, F | 1 |
| Klocker, H | 2 |
| Cato, AC | 2 |
| Bøtker, HE | 1 |
| Møller, N | 1 |
| Ovesen, P | 1 |
| Mengel, A | 1 |
| Schmitz, O | 1 |
| Orskov, H | 1 |
| Bagger, JP | 1 |
| Kaspar, F | 1 |
| Denninger, A | 1 |
| Philen, RM | 1 |
| Hill, RH | 1 |
| Gallardo, S | 1 |
| Cárdaba, B | 1 |
| del Pozo, V | 1 |
| de Andrés, B | 1 |
| Cortegano, I | 1 |
| Jurado, A | 1 |
| Tramón, P | 1 |
| Palomino, P | 1 |
| Lahoz, C | 1 |
| Klannemark, M | 1 |
| Orho, M | 1 |
| Groop, L | 1 |
| Satoda, M | 1 |
| Zhao, F | 1 |
| Diaz, GA | 1 |
| Burn, J | 1 |
| Goodship, J | 1 |
| Davidson, HR | 1 |
| Pierpont, ME | 1 |
| Gelb, BD | 1 |
| Jang, IK | 1 |
| Newby, LK | 1 |
| McGuire, DK | 1 |
| DeVivo, DC | 1 |
| Haymond, MW | 1 |
| Obert, KA | 1 |
| Nelson, JS | 1 |
| Pagliara, AS | 1 |
| Tada, K | 1 |
| Takada, G | 1 |
| Omura, K | 1 |
| Itokawa, Y | 1 |
| Fischer, MH | 1 |
| Fortune, JS | 1 |
| Foster, SH | 1 |
| Gilbert, EF | 1 |
| von Schenck, H | 1 |
| Thorell, JI | 1 |
| Berg, J | 1 |
| Bojs, G | 1 |
| Dymling, JF | 1 |
| Hallengren, B | 1 |
| Ljungberg, O | 1 |
| Tibblin, S | 1 |
| Gröbe, H | 1 |
| Bassewitz, DB | 1 |
| Dominick, HC | 1 |
| Pfeiffer, RA | 1 |
| Beaudry, MA | 1 |
| Letarte, J | 1 |
| Collu, R | 1 |
| Leboeuf, G | 1 |
| Ducharme, JR | 1 |
| Melancon, SB | 1 |
| Dallairf, L | 1 |
| Sasaki, H | 1 |
| Matsuda, M | 1 |
| Terasawa, T | 1 |
| Ito, T | 1 |
| Fukushima, Y | 1 |
| Kuroki, Y | 1 |
| Matsuyama, S | 1 |
| Simell, O | 1 |
| Mackenzie, S | 1 |
| Clow, CL | 1 |
| Scriver, CR | 1 |
| Hansson, UB | 1 |
| Lindström, FD | 1 |
| Dotchev, D | 1 |
| Hungerland, H | 1 |
| Liappis, N | 1 |
| Oyanagi, K | 1 |
| Felig, P | 2 |
| Havel, RJ | 2 |
| Jorfeldt, L | 2 |
| Pernow, B | 2 |
| Saltin, B | 2 |
| Wahren, J | 2 |
| Donnelly, PE | 1 |
| Turtle, JR | 1 |
| Niemeyer, G | 1 |
| Marquardt, JL | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| In-vivo Thrombus Imaging With 18F-GP1, a Novel Platelet PET Radiotracer[NCT03943966] | 73 participants (Actual) | Interventional | 2019-11-11 | Completed | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
2 reviews available for alanine and Syndrome
| Article | Year |
|---|---|
The use of glycoprotein IIb/IIIa inhibitors in patients with coronary artery disease.
Topics: Abciximab; Acetates; Acute Disease; Administration, Oral; Alanine; Angioplasty, Balloon, Coronary; A | 2000 |
Oral platelet glycoprotein IIb/IIIa inhibition.
Topics: Alanine; Angina, Unstable; Aspirin; Benzamidines; Clinical Trials, Phase II as Topic; Clinical Trial | 2000 |
2 trials available for alanine and Syndrome
| Article | Year |
|---|---|
Risk factors for stroke after acute coronary syndromes in the Orbofiban in Patients with Unstable Coronary Syndromes--Thrombolysis In Myocardial Infarction (OPUS-TIMI) 16 study.
Topics: Aged; Alanine; Angina, Unstable; Aspirin; Cerebral Hemorrhage; Female; Fibrinolytic Agents; Follow-U | 2006 |
Clinical application of C-reactive protein across the spectrum of acute coronary syndromes.
Topics: Acute Disease; Aged; Alanine; Angina Pectoris; Angina, Unstable; C-Reactive Protein; Coronary Diseas | 2007 |
40 other studies available for alanine and Syndrome
| Article | Year |
|---|---|
Hepatobiliary and Pancreatic: Mauriac syndrome: A rare cause of elevated liver enzymes.
Topics: Adolescent; Alanine; Alanine Transaminase; Aspartate Aminotransferases; Diabetes Mellitus, Type 1; F | 2019 |
Prevalent polymorphism in thyroid hormone-activating enzyme leaves a genetic fingerprint that underlies associated clinical syndromes.
Topics: Adult; Alanine; Amino Acid Substitution; Case-Control Studies; Cerebral Cortex; Gene Frequency; HEK2 | 2015 |
Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.
Topics: Alanine; Amelogenesis Imperfecta; Base Sequence; Child; Codon, Nonsense; Cytosine; Dental Enamel Pro | 2015 |
Introduction into Ca(v)2.1 of the homologous mutation of Ca(v)1.2 causing the Timothy syndrome questions the role of V421 in the phenotypic definition of P-type Ca(2+) channel.
Topics: Alanine; Animals; Arginine; Arrhythmias, Cardiac; Calcium; Calcium Channels, L-Type; Calcium Channel | 2008 |
Novel mutations in the IRF6 gene in Brazilian families with Van der Woude syndrome.
Topics: Alanine; American Indian or Alaska Native; Amino Acid Sequence; Base Sequence; Brazil; Craniofacial | 2008 |
Congenital central hypoventilation syndrome: genotype-phenotype correlation in parents of affected children carrying a PHOX2B expansion mutation.
Topics: Adult; Alanine; Child; Child, Preschool; Family Health; Female; Genetic Association Studies; Homeodo | 2010 |
A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.
Topics: Acidosis, Lactic; Adult; Alanine; Brain Ischemia; DNA, Mitochondrial; Glycine; Humans; Male; MELAS S | 2011 |
DEND syndrome due to V59A mutation in KCNJ11 gene: unresponsive to sulfonylureas.
Topics: Alanine; Amino Acid Substitution; Diabetes Mellitus; Epilepsies, Myoclonic; Female; Humans; Hypoglyc | 2013 |
Evaluation of the AccuTnI cardiac troponin I assay for risk assessment in acute coronary syndromes.
Topics: Acute Disease; Alanine; Biomarkers; Coronary Disease; Female; Humans; Immunoassay; Male; Middle Aged | 2003 |
MICA association with presumed ocular histoplasmosis syndrome (POHS).
Topics: Adult; Alanine; Eye Infections, Fungal; Female; Histocompatibility Antigens Class I; Histoplasma; Hi | 2003 |
Identification of two novel mutations of IRF6 in Korean families affected with Van der Woude syndrome.
Topics: Alanine; Amino Acid Sequence; Cleft Lip; Cleft Palate; Codon; DNA-Binding Proteins; Frameshift Mutat | 2003 |
[Behavior of certain enzymatic activities in the course of ischemic syndromes due to obstructive arteriopathies of the lower extremities (aspartic & alanine-ketoglutaric transaminases, phosphoglucomutases)].
Topics: Alanine; Alanine Transaminase; Intramolecular Transferases; Lower Extremity; Peripheral Vascular Dis | 1959 |
Does initial and delayed heart rate predict mortality in patients with acute coronary syndromes?
Topics: Acute Disease; Alanine; Female; Heart Rate; Humans; Male; Middle Aged; Myocardial Infarction; Platel | 2004 |
Statins are associated with lower risk of gastrointestinal bleeding in patients with unstable coronary syndromes: analysis of the Orbofiban in Patients with Unstable coronary Syndromes-Thrombolysis In Myocardial Infarction 16 (OPUS-TIMI 16) trial.
Topics: Acute Disease; Administration, Oral; Aged; Alanine; Anticoagulants; Aspirin; Coronary Disease; Femal | 2006 |
Parsing ketotic hypoglycaemia.
Topics: Alanine; Child, Preschool; Fasting; Glycogen Synthase; Humans; Hypoglycemia; Infant; Insulin; Ketosi | 2006 |
Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.
Topics: Alanine; Homeodomain Proteins; Humans; Models, Molecular; Mutation; Pedigree; Promoter Regions, Gene | 2007 |
Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome.
Topics: Abnormalities, Multiple; Adult; Alanine; Anterior Eye Segment; Asian People; Base Sequence; Child, P | 2007 |
Structural basis for reduced FGFR2 activity in LADD syndrome: Implications for FGFR autoinhibition and activation.
Topics: Abnormalities, Multiple; Adenosine Triphosphate; Alanine; Crystallography, X-Ray; Humans; Models, Mo | 2007 |
A single amino acid exchange abolishes dimerization of the androgen receptor and causes Reifenstein syndrome.
Topics: Alanine; Base Sequence; Binding Sites; Cell Line; DNA; Humans; Macromolecular Substances; Molecular | 1995 |
Insulin resistance in microvascular angina (syndrome X)
Topics: Alanine; Angina Pectoris; Basal Metabolism; Blood Glucose; C-Peptide; Chest Pain; Coronary Circulati | 1993 |
A mutant androgen receptor from patients with Reifenstein syndrome: identification of the function of a conserved alanine residue in the D box of steroid receptors.
Topics: Alanine; Amino Acid Sequence; Animals; Base Sequence; Binding Sites; Conserved Sequence; DNA; Humans | 1993 |
3-(Phenylamino)alanine--a link between eosinophilia-myalgia syndrome and toxic oil syndrome?
Topics: Alanine; Brassica; Eosinophilia-Myalgia Syndrome; Fatty Acids, Monounsaturated; Food Contamination; | 1993 |
Study of apoptosis in human lymphocytes by toxic substances implicated in toxic oil syndrome.
Topics: Alanine; Aniline Compounds; Apoptosis; Brassica; Cells, Cultured; Coloring Agents; DNA; Dose-Respons | 1997 |
No relationship between identified variants in the uncoupling protein 2 gene and energy expenditure.
Topics: Aged; Alanine; Amino Acid Substitution; Energy Metabolism; Exons; Female; Genetic Variation; Genotyp | 1998 |
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus.
Topics: 3T3 Cells; Abnormalities, Multiple; Alanine; Amino Acid Sequence; Animals; Aspartic Acid; Cell Line; | 2000 |
Learning from the recently completed oral glycoprotein IIb/IIIa receptor antagonist trials.
Topics: Alanine; Angina, Unstable; Benzamidines; Humans; Myocardial Infarction; Platelet Aggregation Inhibit | 2000 |
Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (Leigh disease).
Topics: Alanine; Blood Glucose; Brain; Brain Diseases; Decarboxylation; Dichloroacetic Acid; Enzyme Activati | 1979 |
Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase.
Topics: Acidosis; Alanine; Brain Stem; Child, Preschool; Encephalomalacia; Female; Humans; Infant; Intellect | 1978 |
Chemical analysis of an angiofibroma from a patient with tuberous sclerosis.
Topics: Adult; Alanine; Collagen; Dermatan Sulfate; Facial Neoplasms; Galactosidases; Glucuronidase; Glycine | 1977 |
Metabolic studies and glucagon gel filtration pattern before and after surgery in a case of glucagonoma syndrome.
Topics: Adenoma, Islet Cell; Aged; Alanine; Anemia; Arginine; Chromatography, Gel; Erythema; Glossitis; Gluc | 1979 |
Subacute necrotizing encephalomyelopathy. Clinical, ultrastructural, biochemical and therapeutic studies in an infant.
Topics: Alanine; Brain Stem; Encephalomalacia; Female; Glycogen; Humans; Infant; Intellectual Disability; La | 1975 |
[Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)].
Topics: Alanine; Amino Acids; Ammonia; Child, Preschool; Dietary Proteins; Erythrocytes; Growth Disorders; H | 1975 |
[Analysis of the relative rates of synthesis of G gamma and A gamma globin chains in the erythropoietic bursts in patients with trisomy 13 syndrome].
Topics: Alanine; Chromosomes, Human, Pair 13; Erythroid Precursor Cells; Female; Fetal Hemoglobin; Globins; | 1989 |
Ornithine loading did not prevent induced hyperammonemia in a patient with hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Child; Citrulline; Cytoplasm; H | 1985 |
Some factors affecting precipitation and complex formation of an IgG cryoglobulin.
Topics: Adult; Alanine; Albumins; Antigen-Antibody Complex; Blood Protein Electrophoresis; Blood Sedimentati | 1973 |
[Hyperiminoaciduria and disaminoaciduria in endemic (Balkan-)nephropathy (author's transl)].
Topics: Adult; Aged; Alanine; Amino Acids; Chromatography, Thin Layer; Chronic Disease; Creatinine; Female; | 1974 |
Amino acid metabolism during exercise in McArdle's syndrome: evidence of altered alanine metabolism.
Topics: Alanine; Amino Acids; Glucosyltransferases; Glycogen Storage Disease; Humans; Muscles; Muscular Dise | 1972 |
Amino acid metabolism in McArdle's syndrome.
Topics: Adult; Alanine; Amino Acids; Glucosyltransferases; Glycogen Storage Disease; Humans; Leg; Male; Musc | 1973 |
Ketotic hypoglycaemia due to hypoalaninaemia.
Topics: Acidosis; Alanine; Child; Gluconeogenesis; Humans; Hypoglycemia; Male; Metabolic Diseases; Syndrome | 1974 |
Retinal function in an unique syndrome of optic atrophy, juvenile diabetes mellitus, diabetes insipidus, neurosensory hearing loss, autonomic dysfunction, and hyperalanineuria.
Topics: Adaptation, Ocular; Adult; Alanine; Amino Acid Metabolism, Inborn Errors; Diabetes Insipidus; Diabet | 1972 |