Compounds > homocysteine

homocysteine and Marfan Syndrome, Type I

homocysteine has been researched along with Marfan Syndrome, Type I in 16 studies

Research

Studies (16)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (12.50)	18.7374
1990's	1 (6.25)	18.2507
2000's	9 (56.25)	29.6817
2010's	4 (25.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Camargo, EC; Huang, SY; Karaa, A; Rosenbaum, MW	1
Ágg, B; Benke, K; Harsányi, G; Mátyás, G; Maurovich-Horvat, P; Merkely, B; Nagy, ZB; Odler, B; Pólos, M; Radovits, T; Szabolcs, Z; Szilveszter, B; Szokolai, V	1
Cirulis, JT; Hubmacher, D; Keeley, FW; Miao, M; Reinhardt, DP	1
Dietzen, DJ; Oladipo, O; Shinawi, M; Spreitsma, L	1
Abbate, R; Brunelli, T; Evangelisti, L; Fedi, S; Gensini, GF; Giusti, B; Pepe, G; Porciani, MC; Sani, G; Yacoub, M	1
Kotel'nikov, MV	1
Janel, N; Maurin, N; Robert, K; Siauve, N; Vayssettes, C	1
Giusti, B; Lapini, I; Lenti, M; Marcucci, R; Pepe, G; Sestini, I; Yacoub, M	1
Aplin, RT; Boers, GH; Handford, PA; Hutchinson, S; Kettle, S; Timmermans, J; Webb, H	1
Takagi, H; Umemoto, T	1
Bartels, R; Bätge, B; Brinckmann, J; Hubmacher, D; Notbohm, H; Reinhardt, DP; Tiedemann, K; Vollbrandt, T	1
Alscher, DM; Benzinger, P	1
Blom, HJ; Heil, SG; Hogeveen, M; Kluijtmans, LA; Morava, E; van de Berg, GB; van Dijken, PJ	1
Artuch, R; Camacho, JA; Campistol, J; Cardo, E; Ferrer, I; Moyano, D; Pavia, C; Pineda, M; Vilaseca, MA	1
Sviatkina, OB; Vel'tishchev, IuE	1
Stone, JH	1

Reviews

3 review(s) available for homocysteine and Marfan Syndrome, Type I

Article	Year
[Hyperhomocysteinemia: from theory and practice in the treatment of thrombophilias]. Kardiologiia, 2004, Volume: 44, Issue:10 Topics: Administration, Oral; Anticoagulants; Blood Coagulation Tests; Cardiovascular Diseases; Double-Blind Method; Drug Therapy, Combination; Folic Acid; Homocysteine; Humans; Hyperhomocysteinemia; Marfan Syndrome; Multicenter Studies as Topic; Mutation; Polymorphism, Genetic; Randomized Controlled Trials as Topic; Risk Factors; Thrombophilia; Time Factors; Venous Thrombosis; Vitamin B 12; Vitamin B 6	2004
Role of hyperhomocysteinemia in aortic disease. Cellular and molecular biology (Noisy-le-Grand, France), 2004, Volume: 50, Issue:8 Topics: Aged; Animals; Aorta; Aortic Aneurysm, Abdominal; Aortic Diseases; Collagen; Disease Progression; Extracellular Matrix; Female; Fibrillin-1; Fibrillins; Genotype; Homocysteine; Humans; Hyperhomocysteinemia; Male; Marfan Syndrome; Microfilament Proteins; Middle Aged; Risk; Thrombosis; Vascular Diseases	2004
[Hereditary anomalies of methionine metabolism in children]. Pediatriia, 1972, Volume: 51, Issue:4 Topics: Age Factors; Child; Flatfoot; Folic Acid; Homocysteine; Homocystine; Homocystinuria; Humans; Intellectual Disability; Kyphosis; Marfan Syndrome; Metabolism, Inborn Errors; Methionine; Scoliosis	1972

Other Studies

13 other study(ies) available for homocysteine and Marfan Syndrome, Type I

Article	Year
Case 7-2018: A 25-Year-Old Man with New-Onset Seizures. The New England journal of medicine, 2018, Mar-08, Volume: 378, Issue:10 Topics: Adult; Brain; Brain Edema; Diagnosis, Differential; Homocysteine; Homocystinuria; Humans; Magnetic Resonance Imaging; Male; Marfan Syndrome; Seizures; Sinus Thrombosis, Intracranial; Tomography, X-Ray Computed	2018
Gene polymorphisms as risk factors for predicting the cardiovascular manifestations in Marfan syndrome. Role of folic acid metabolism enzyme gene polymorphisms in Marfan syndrome. Thrombosis and haemostasis, 2015, Volume: 114, Issue:4 Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adolescent; Adult; Aortic Aneurysm; Aortic Dissection; Biomarkers; Case-Control Studies; Chi-Square Distribution; Female; Ferredoxin-NADP Reductase; Folic Acid; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Heterozygote; Homocysteine; Homozygote; Humans; Logistic Models; Male; Marfan Syndrome; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Multivariate Analysis; Odds Ratio; Phenotype; Polymorphism, Single Nucleotide; Predictive Value of Tests; Risk Factors; Severity of Illness Index; Up-Regulation; Vitamin B 12; Young Adult	2015
Functional consequences of homocysteinylation of the elastic fiber proteins fibrillin-1 and tropoelastin. The Journal of biological chemistry, 2010, Jan-08, Volume: 285, Issue:2 Topics: Cells, Cultured; Cystathionine beta-Synthase; Ectopia Lentis; Fibrillin-1; Fibrillins; Fibroblasts; Homocysteine; Homocystinuria; Humans; Marfan Syndrome; Microfilament Proteins; Mutation; Protein Multimerization; Protein Processing, Post-Translational; Protein Structure, Tertiary; Scoliosis; Tropoelastin	2010
Increased homocysteine in a patient diagnosed with Marfan syndrome. Clinical chemistry, 2010, Volume: 56, Issue:11 Topics: Cystathionine beta-Synthase; Diagnosis, Differential; Female; Homocysteine; Homocystinuria; Humans; Marfan Syndrome; Methionine; Middle Aged; Mutation	2010
Phenotypic variability of cardiovascular manifestations in Marfan Syndrome. Possible role of hyperhomocysteinemia and C677T MTHFR gene polymorphism. European heart journal, 2003, Volume: 24, Issue:22 Topics: Adolescent; Adult; Aortic Aneurysm; Aortic Dissection; Cardiovascular Diseases; Female; Homocysteine; Humans; Hyperhomocysteinemia; Logistic Models; Male; Marfan Syndrome; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Phenotype; Polymorphism, Genetic; Severity of Illness Index	2003
Cystathionine beta synthase deficiency affects mouse endochondral ossification. The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology, 2005, Volume: 282, Issue:1 Topics: Animals; Bone and Bones; Breeding; Cystathionine beta-Synthase; Disease Models, Animal; DNA; Female; Genotype; Homocysteine; Hyperhomocysteinemia; Male; Marfan Syndrome; Mice; Mice, Inbred Strains; Mice, Knockout; Osteogenesis; Radiography; Scoliosis	2005
Molecular effects of homocysteine on cbEGF domain structure: insights into the pathogenesis of homocystinuria. Journal of molecular biology, 2005, Feb-25, Volume: 346, Issue:3 Topics: Calcium; Cystathionine beta-Synthase; Epidermal Growth Factor; Fibrillin-1; Fibrillins; Homocysteine; Homocystinuria; Humans; In Vitro Techniques; Marfan Syndrome; Microfilament Proteins; Models, Molecular; Oxidation-Reduction; Peptide Fragments; Protein Folding; Protein Structure, Tertiary; Receptor, Notch1; Receptors, Cell Surface; Recombinant Proteins; Spectrometry, Mass, Electrospray Ionization; Transcription Factors; Trypsin	2005
Homocysteinemia is a risk factor for aortic dissection. Medical hypotheses, 2005, Volume: 64, Issue:5 Topics: Aortic Rupture; Homocysteine; Humans; Marfan Syndrome; Risk Factors	2005
Modification of the structure and function of fibrillin-1 by homocysteine suggests a potential pathogenetic mechanism in homocystinuria. The Journal of biological chemistry, 2005, Oct-14, Volume: 280, Issue:41 Topics: Amino Acid Sequence; Calcium; Cells, Cultured; Chymotrypsin; Circular Dichroism; Dose-Response Relationship, Drug; Epidermal Growth Factor; Extracellular Matrix; Fibrillin-1; Fibrillins; Fibroblasts; Glycosylation; Homocysteine; Homocystinuria; Humans; Marfan Syndrome; Microfilament Proteins; Microscopy, Fluorescence; Molecular Sequence Data; Peptides; Protein Binding; Protein Conformation; Protein Structure, Secondary; Protein Structure, Tertiary; Recombinant Proteins; Sequence Homology, Amino Acid; Transfection; Trypsin	2005
[Untreated homocystinuria in adulthood]. Deutsche medizinische Wochenschrift (1946), 2005, Oct-28, Volume: 130, Issue:43 Topics: Adult; Age Factors; Angina Pectoris; Betaine; Diagnosis, Differential; Drug Therapy, Combination; Folic Acid; Homocysteine; Homocystine; Homocystinuria; Humans; Intervertebral Disc Displacement; Lens Subluxation; Male; Marfan Syndrome; Myopia; Osteoporosis; Retinal Detachment; Vitamin B 12; Vitamin B 6; Vitamin B Complex	2005
Marfanoid features in a child with combined methylmalonic aciduria and homocystinuria (CblC type). Journal of inherited metabolic disease, 2007, Volume: 30, Issue:5 Topics: Adolescent; Carnitine; Carrier Proteins; Child; Cysteine; Diagnosis, Differential; DNA Mutational Analysis; Exons; Female; Folic Acid; Genetic Testing; Heterozygote; Homocysteine; Homocystinuria; Humans; Male; Marfan Syndrome; Metabolism, Inborn Errors; Methylmalonic Acid; Mutation; Oxidoreductases; Pedigree; Phenotype; Treatment Outcome; Vitamin B 12; Vitamin B 6; Vitamins	2007
Selective screening for hyperhomocysteinemia in pediatric patients. Clinical chemistry, 1998, Volume: 44, Issue:3 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Anemia, Megaloblastic; Anorexia Nervosa; Cardiovascular Diseases; Child; Child, Preschool; Cystathionine beta-Synthase; Diabetes Mellitus, Type 1; Environment; Homocysteine; Humans; Infant; Marfan Syndrome; Mass Screening; Reference Values; Renal Insufficiency; Risk Factors	1998
Ectopia lentis, cardiology, and "the sign of the tremulous iris". American heart journal, 1966, Volume: 72, Issue:4 Topics: Cardiovascular Diseases; Collagen Diseases; Eye Injuries; Homocysteine; Humans; Iris; Lens, Crystalline; Marfan Syndrome; Ophthalmoscopy	1966