khellin has been researched along with Abnormalities, Multiple in 15 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.
Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Polyfibromatosis is a rare fibrosing condition characterized by fibromatosis in different body areas and by keloid formation, and which can be associated with arthropathy and osteolysis." | 1.39 | Arthropathy, osteolysis, keloids, relapsing conjunctival pannus and gingival overgrowth: a variant of polyfibromatosis? ( Cinotti, E; Di Maria, E; Faravelli, F; Ferrero, G; Papadia, M; Paparo, F; Rongioletti, F; Traverso, C, 2013) |
| "The array of malignant neoplasms does not suggest an etiology or pathogenesis in common." | 1.28 | Keloids and neoplasms in the Rubinstein-Taybi syndrome. ( Miller, RW; Rubinstein, JH; Siraganian, PA, 1989) |
| "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 | 7 (46.67) | 18.7374 |
| 1990's | 2 (13.33) | 18.2507 |
| 2000's | 4 (26.67) | 29.6817 |
| 2010's | 2 (13.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cinotti, E | 1 |
| Ferrero, G | 1 |
| Paparo, F | 1 |
| Papadia, M | 1 |
| Faravelli, F | 1 |
| Rongioletti, F | 1 |
| Traverso, C | 1 |
| Di Maria, E | 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 |
| Archer, HL | 1 |
| Gupta, S | 1 |
| Enoch, S | 1 |
| Thompson, P | 1 |
| Rowbottom, A | 1 |
| Chua, I | 1 |
| Warren, S | 1 |
| Johnson, D | 1 |
| Ledbetter, DH | 1 |
| Lese-Martin, C | 1 |
| Williams, P | 1 |
| Pilz, DT | 1 |
| Ricart, J | 1 |
| Pareja, IE | 1 |
| Zuffardi, O | 1 |
| Fraccaro, M | 1 |
| Selmanowitz, VJ | 1 |
| Stiller, MJ | 1 |
| Goodfellow, A | 1 |
| Emmerson, RW | 1 |
| Calvert, HT | 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 |
| Kurwa, AR | 1 |
| Siraganian, PA | 1 |
| Rubinstein, JH | 1 |
| Miller, RW | 1 |
| Sammartino, A | 1 |
| Cerbella, R | 1 |
| Lembo, G | 1 |
| Federico, A | 1 |
| Loffredo, L | 1 |
| Rohlfing, B | 1 |
| Lewis, K | 1 |
| Singleton, EB | 1 |
1 review available for khellin and Abnormalities, Multiple
| Article | Year |
|---|---|
Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter.
Topics: Abnormalities, Multiple; Adolescent; Chromosome Deletion; Chromosomes, Human, Pair 19; Cleft Palate; | 2005 |
14 other studies available for khellin and Abnormalities, Multiple
| Article | Year |
|---|---|
Arthropathy, osteolysis, keloids, relapsing conjunctival pannus and gingival overgrowth: a variant of polyfibromatosis?
Topics: Abnormalities, Multiple; Arthrography; Cleft Palate; Comparative Genomic Hybridization; Conjunctival | 2013 |
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 |
Trisomy 9p associated with self-injured behaviour and multiple intractable keloids.
Topics: Abnormalities, Multiple; Adult; Chromosomes, Human, Pair 9; Female; Humans; Keloid; Self-Injurious B | 2006 |
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 |
Rubinstein-Taybi syndrome. Cutaneous manifestations and colossal keloids.
Topics: Abnormalities, Multiple; Adult; Female; Humans; Keloid; Rubinstein-Taybi Syndrome; Skin; Skin Abnorm | 1981 |
Rubinstein-Taybi syndrome and spontaneous keloids.
Topics: Abnormalities, Multiple; Adult; Humans; Keloid; Male; Rubinstein-Taybi Syndrome | 1980 |
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 |
Rubinstein-Taybi syndrome and spontaneous keloids.
Topics: Abnormalities, Multiple; Adult; Female; Humans; Keloid; Rubinstein-Taybi Syndrome | 1979 |
Keloids and neoplasms in the Rubinstein-Taybi syndrome.
Topics: Abnormalities, Multiple; Adolescent; Adult; Child; Child, Preschool; Female; Humans; Infant; Infant, | 1989 |
[Rubinstein-Taybi syndrome with multiple keloids].
Topics: Abnormalities, Multiple; Adolescent; Female; Humans; Keloid; Pedigree; Phenotype; Rubinstein-Taybi S | 1986 |
Rubinstein-Taybi syndrome. Report of an unusual case.
Topics: Abnormalities, Multiple; Adult; Bone and Bones; Cleft Palate; Elbow; Face; Female; Humans; Intellect | 1971 |