khellin has been researched along with Syndrome in 13 studies
Khellin: A vasodilator that also has bronchodilatory action. It has been employed in the treatment of angina pectoris, in the treatment of asthma, and in conjunction with ultraviolet light A, has been tried in the treatment of vitiligo. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1024)
khellin : A furanochrome in which the basic tricyclic skeleton is substituted at positions 4 and 9 with methoxy groups and at position 7 with a methyl group. A major constituent of the plant Ammi visnaga it is a herbal folk medicine used for various illnesses, its main effect being as a vasodilator.
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Keloids are proliferative fibrous growths that result from an excessive tissue response to skin trauma." | 1.31 | Clinical genetics of familial keloids. ( Marneros, AG; Norris, JE; Olsen, BR; Reichenberger, E, 2001) |
| "The syndrome of torticollis, keloids, cryptorchidism and renal dysplasia was described by Goeminne (1968) in a large family, and listed as X-linked incomplete dominant by McKusick (1978; No." | 1.26 | Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, Mckusick) is at Xq28, distal to the G6PD locus. ( Fraccaro, M; Zuffardi, O, 1982) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (46.15) | 18.7374 |
| 1990's | 2 (15.38) | 18.2507 |
| 2000's | 3 (23.08) | 29.6817 |
| 2010's | 2 (15.38) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Atwal, PS | 1 |
| Blease, S | 1 |
| Braxton, A | 1 |
| Graves, J | 1 |
| He, W | 1 |
| Person, R | 1 |
| Slattery, L | 1 |
| Bernstein, JA | 1 |
| Hudgins, L | 1 |
| Heyen, CA | 1 |
| Delk, PR | 1 |
| Bull, MJ | 1 |
| Weaver, DD | 1 |
| Eberwein, P | 1 |
| Reinhard, T | 1 |
| Agostini, H | 1 |
| Poloschek, CM | 1 |
| Guthoff, R | 1 |
| Auw-Haedrich, C | 1 |
| Fryns, JP | 1 |
| Gevers, D | 1 |
| DESFORGES, JA | 1 |
| Zuffardi, O | 1 |
| Fraccaro, M | 1 |
| Zaĭtseva, SIu | 1 |
| Trofimova, IB | 1 |
| Paradisi, M | 1 |
| Angelo, C | 1 |
| Conti, G | 1 |
| Mostaccioli, S | 1 |
| Cianchini, G | 1 |
| Atzori, F | 1 |
| Puddu, P | 1 |
| Elia, M | 1 |
| Di Lello, R | 1 |
| Romano, C | 1 |
| Schepis, C | 1 |
| Marneros, AG | 1 |
| Norris, JE | 1 |
| Olsen, BR | 1 |
| Reichenberger, E | 1 |
| Elsas, FJ | 1 |
| Green, WR | 1 |
| Rumi, TK | 1 |
| Kapkaev, RA | 1 |
| Sampaio, MM | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Identification of Genetic Variants That Contribute to Keloid Formation in Families and Isolated Cases.[NCT01619553] | 7,000 participants (Anticipated) | Observational | 2009-04-30 | Recruiting | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
13 other studies available for khellin and Syndrome
| Article | Year |
|---|---|
Novel X-linked syndrome of cardiac valvulopathy, keloid scarring, and reduced joint mobility due to filamin A substitution G1576R.
Topics: Adult; Alleles; Amino Acid Substitution; Codon; Facies; Filamins; Genetic Association Studies; Genet | 2016 |
A report of an apparent new genetic syndrome consisting of joint contractures, keloids, large optic cup-to-disc ratio and renal stones.
Topics: Abnormalities, Multiple; Adult; Child; Contracture; Female; Humans; Joints; Keloid; Kidney Calculi; | 2008 |
[Intensive intracorneal keloid formation in a case of Peters plus syndrome and in Peters anomaly with maximum manifestation].
Topics: Abnormalities, Multiple; Cataract; Cornea; Corneal Diseases; Eye Abnormalities; Female; Humans; Infa | 2010 |
Goeminne syndrome (OMIM 314300): another male patient 30 years later.
Topics: Abnormalities, Multiple; Adult; Cervical Vertebrae; Chromosomes, Human, X; Cryptorchidism; Follow-Up | 2003 |
Non-surgical reduction of granuloma and keloids.
Topics: Fibroma; Foot; Foot Diseases; Granuloma; Humans; Hydrocortisone; Keloid; Neoplasms; Syndrome | 1958 |
Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, Mckusick) is at Xq28, distal to the G6PD locus.
Topics: Abnormalities, Multiple; Chromosome Mapping; Cryptorchidism; Female; Glucosephosphate Dehydrogenase; | 1982 |
[2 cases of keloid diathesis in one family].
Topics: Adult; Disease Susceptibility; Epilepsy; Female; Heart Defects, Congenital; Humans; Keloid; Male; Sy | 1982 |
Dubowitz syndrome with keloidal lesions.
Topics: Abnormalities, Multiple; Child; Dermatitis, Atopic; Facial Expression; Growth Disorders; Humans; Kel | 1994 |
A case of FG syndrome with gingival hyperplasia and keloids.
Topics: Abnormalities, Multiple; Child; Gingival Hyperplasia; Humans; Keloid; Male; Syndrome | 1995 |
Clinical genetics of familial keloids.
Topics: Adolescent; Adult; Age of Onset; Black People; Child; Diseases in Twins; Female; Genes, Dominant; Hu | 2001 |
Epibulbar tumors in childhood.
Topics: Adolescent; Amyloidosis; Carcinoma, Squamous Cell; Child; Child, Preschool; Choristoma; Conjunctiva; | 1975 |
[Keloidal blastomycosis (Lobo's disease)].
Topics: Adolescent; Biopsy; Blastomycosis; Combined Modality Therapy; Diagnosis, Differential; Humans; Keloi | 1988 |
A note on the cultivation of the aetiological agent of Jorge Lôbo's disease in 199 T.C. medium containing phytohaemagglutinin. Preliminary report.
Topics: Blastomyces; Blastomycosis; Culture Media; Humans; Keloid; Lectins; Syndrome | 1974 |