salicylic acid has been researched along with Hypotrichosis in 39 studies
Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).
Hypotrichosis: Presence of less than the normal amount of hair. (Dorland, 27th ed)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Gentamicin was further shown to rescue corneodesmosin translation in primary keratinocytes obtained from a patient with HSS." | 6.94 | Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin. ( Bochner, R; Malki, L; Pavlovsky, M; Peled, A; Pichinuk, E; Samuelov, L; Sarig, O; Sprecher, E; Weil, M, 2020) |
| "Gentamicin was further shown to rescue corneodesmosin translation in primary keratinocytes obtained from a patient with HSS." | 2.94 | Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin. ( Bochner, R; Malki, L; Pavlovsky, M; Peled, A; Pichinuk, E; Samuelov, L; Sarig, O; Sprecher, E; Weil, M, 2020) |
| "Ichthyosis is a heterogeneous group of skin disorders characterized by abnormal epidermal scaling." | 1.31 | Homozygosity mapping of a locus for a novel syndromic ichthyosis to chromosome 3q27-q28. ( Baala, L; Courtois, G; De Prost, Y; Hadchouel, M; Hadj-Rabia, S; Hamel-Teillac, D; Jacquemin, E; Leal, SM; Lyonnet, S; Munnich, A; Prost, C; Sefiani, A; Vabres, P, 2002) |
| "Gonosomal aberrations such as Turner's syndrome are frequently associated with autoimmune diseases or with serological markers for autoimmune diseases." | 1.29 | [Alopecia areata and diffuse hypotrichosis associated with Ullrich-Turner syndrome. Presentation of 4 patients]. ( Gollnick, H; Müller, R; Orfanos, CE; Reupke, HJ; Tebbe, B, 1993) |
| "A case of naevoid hypotrichosis affecting two symmetrical areas in the parietal regions is described." | 1.27 | Focal naevoid hypotrichosis. ( Barth, JH; Dawber, RP, 1987) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (17.95) | 18.7374 |
| 1990's | 4 (10.26) | 18.2507 |
| 2000's | 10 (25.64) | 29.6817 |
| 2010's | 11 (28.21) | 24.3611 |
| 2020's | 7 (17.95) | 2.80 |
| Authors | Studies |
|---|---|
| López-Balboa, P | 1 |
| Martos-Cabrera, L | 1 |
| Ramírez-Lluch, M | 1 |
| Noguera-Morel, L | 1 |
| Ortiz-Cabrera, NV | 1 |
| González-Sarmiento, R | 1 |
| Torrelo, A | 1 |
| Hernández-Martín, Á | 1 |
| Vastarella, M | 1 |
| Martora, F | 1 |
| Ocampo-Garza, S | 1 |
| Patri, A | 1 |
| Battista, T | 1 |
| Nappa, P | 1 |
| Fabbrocini, G | 1 |
| Cantelli, M | 1 |
| Rayinda, T | 1 |
| McSweeney, SM | 1 |
| Lalagianni, N | 1 |
| Liu, L | 1 |
| Guy, A | 1 |
| Fenton, D | 1 |
| Stefanato, CM | 1 |
| Dand, N | 1 |
| McGrath, JA | 1 |
| Tziotzios, C | 1 |
| de Abreu, EP | 1 |
| Rocha, VB | 1 |
| Queiroz de Melo, RF | 1 |
| Pereira, LB | 1 |
| Peled, A | 1 |
| Samuelov, L | 1 |
| Sarig, O | 1 |
| Bochner, R | 1 |
| Malki, L | 1 |
| Pavlovsky, M | 1 |
| Pichinuk, E | 1 |
| Weil, M | 1 |
| Sprecher, E | 2 |
| Kibbi, N | 1 |
| Rajan, N | 1 |
| Taki, T | 1 |
| Tanahashi, K | 1 |
| Takeichi, T | 1 |
| Yoshikawa, T | 1 |
| Murase, Y | 1 |
| Sugiura, K | 1 |
| Akiyama, M | 1 |
| Farah, RS | 1 |
| Holahan, HM | 1 |
| Moye, MS | 1 |
| Stone, MS | 1 |
| Swick, BL | 1 |
| Huang, H | 1 |
| Sun, J | 1 |
| Fu, L | 1 |
| Wu, J | 1 |
| Guo, H | 1 |
| Yang, C | 1 |
| Zheng, X | 1 |
| Tang, H | 1 |
| Sun, L | 1 |
| Zhang, X | 1 |
| Liu, LH | 1 |
| Wang, JW | 1 |
| Chen, G | 1 |
| Chang, RX | 1 |
| Zhou, Y | 1 |
| Tang, HY | 1 |
| Zhu, J | 1 |
| Wang, PG | 1 |
| Yang, S | 1 |
| Zhang, XJ | 1 |
| Kolb-Mäurer, A | 1 |
| Betz, RC | 5 |
| Hamm, H | 1 |
| Doh, EJ | 1 |
| Yoon, HS | 1 |
| Cho, S | 1 |
| Park, HS | 1 |
| Gentile, P | 1 |
| Garcovich, S | 1 |
| Bielli, A | 1 |
| Scioli, MG | 1 |
| Orlandi, A | 1 |
| Cervelli, V | 1 |
| Barrón-Hernández, YL | 1 |
| Tosti, A | 1 |
| Düzenli, S | 1 |
| Redler, S | 1 |
| Müller, M | 1 |
| Polat, M | 1 |
| Dogruer, D | 1 |
| Pasternack, SM | 1 |
| Shimomura, Y | 1 |
| Agalliu, D | 1 |
| Vonica, A | 1 |
| Luria, V | 1 |
| Wajid, M | 1 |
| Baumer, A | 1 |
| Belli, S | 1 |
| Petukhova, L | 1 |
| Schinzel, A | 1 |
| Brivanlou, AH | 1 |
| Barres, BA | 1 |
| Christiano, AM | 2 |
| Caubet, C | 1 |
| Bousset, L | 1 |
| Clemmensen, O | 1 |
| Sourigues, Y | 1 |
| Bygum, A | 3 |
| Chavanas, S | 1 |
| Coudane, F | 1 |
| Hsu, CY | 1 |
| Melki, R | 1 |
| Simon, M | 2 |
| Serre, G | 2 |
| Nahum, S | 1 |
| Morice-Picard, F | 1 |
| Taieb, A | 1 |
| Huang, XS | 1 |
| Jiang, HO | 1 |
| Quan, QL | 1 |
| Baala, L | 1 |
| Hadj-Rabia, S | 1 |
| Hamel-Teillac, D | 1 |
| Hadchouel, M | 1 |
| Prost, C | 1 |
| Leal, SM | 1 |
| Jacquemin, E | 1 |
| Sefiani, A | 1 |
| De Prost, Y | 1 |
| Courtois, G | 1 |
| Munnich, A | 1 |
| Lyonnet, S | 1 |
| Vabres, P | 1 |
| Levy-Nissenbaum, E | 1 |
| Frydman, M | 1 |
| Lahat, H | 1 |
| Bakhan, T | 1 |
| Goldman, B | 1 |
| Pierick, M | 1 |
| Hillmer, AM | 1 |
| Jonca, N | 1 |
| Toribio, J | 3 |
| Kruse, R | 2 |
| Dewald, G | 1 |
| Cichon, S | 2 |
| Kubisch, C | 1 |
| Guerrin, M | 1 |
| Nöthen, MM | 2 |
| Pras, E | 1 |
| Green, J | 1 |
| Fitzpatrick, E | 1 |
| de Berker, D | 1 |
| Forrest, SM | 1 |
| Sinclair, RD | 1 |
| Sinclair, R | 1 |
| Schaffer, JV | 1 |
| Bazzi, H | 1 |
| Vitebsky, A | 1 |
| Witkiewicz, A | 1 |
| Kovich, OI | 1 |
| Kamino, H | 1 |
| Shapiro, LS | 1 |
| Amin, SP | 1 |
| Orlow, SJ | 1 |
| Kanitakis, J | 1 |
| Tebbe, B | 1 |
| Gollnick, H | 1 |
| Müller, R | 1 |
| Reupke, HJ | 1 |
| Orfanos, CE | 1 |
| Rodríguez Díaz, E | 1 |
| Fernández Blasco, G | 1 |
| Martín Pascual, A | 1 |
| Armijo, M | 1 |
| Glaessl, A | 1 |
| Hohenlautner, U | 1 |
| Landthaler, M | 1 |
| Vogt, T | 1 |
| Lee, YA | 1 |
| Brandrup, F | 2 |
| Bernal, AI | 1 |
| Alvarez, JI | 1 |
| Kukuk, GM | 1 |
| Ibsen, HH | 2 |
| Rasmussen, HB | 1 |
| Wienker, TF | 1 |
| Reis, A | 1 |
| Propping, P | 1 |
| Atasua, M | 1 |
| Dumlu, A | 1 |
| Ozbayrak, S | 1 |
| Spiegl, B | 1 |
| Hundeiker, M | 1 |
| Lazović-Tepavac, O | 1 |
| Gaćinović-Kostanjsek, Z | 1 |
| Korić-Gackić, A | 1 |
| Salamon, T | 1 |
| Clemmensen, OJ | 1 |
| Hess, RO | 1 |
| Uno, H | 1 |
| Barth, JH | 1 |
| Dawber, RP | 1 |
| Dekio, S | 1 |
| Nagashima, T | 1 |
| Watanabe, Y | 1 |
| Jidoi, J | 1 |
| Kohn, G | 1 |
| Metzker, A | 1 |
| Wirth, G | 1 |
| Bindewald, I | 1 |
| Küster, W | 1 |
| Goerz, G | 1 |
| Quiñones, PA | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Biocellular Regenerative Therapy in Treating Scaring Alopecias and Alopecia Areata: Use of High Density Platelet-Rich Plasma Concentrates and Cell-Enriched Emulsified Adipose-Derived Tissue Stromal Vascular Fraction (AD-tSVF)[NCT03078686] | 60 participants (Anticipated) | Interventional | 2017-02-17 | Recruiting | |||
| Evaluating the Efficacy of Different Platelet Rich Plasma (PRP) Treatment Regimens in the Management of Androgenetic Alopecia: an Investigator-initiated, Single-center, Single-blinded, Prospective, Randomized Clinical Trial[NCT02999737] | Phase 4 | 40 participants (Actual) | Interventional | 2016-11-30 | Active, not recruiting | ||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
3 reviews available for salicylic acid and Hypotrichosis
| Article | Year |
|---|---|
Odd-looking hair and progressive alopecia in mother and son.
Topics: Adult; Alopecia; Biopsy, Needle; Disease Progression; Female; Follow-Up Studies; Hair; Heterozygote; | 2014 |
Bimatoprost for the treatment of eyelash, eyebrow and scalp alopecia.
Topics: Alopecia; Bimatoprost; Eyebrows; Eyelashes; Humans; Hypotrichosis; Scalp | 2017 |
Sporadic Bazex-Dupré-Christol-like syndrome: early onset basal cell carcinoma, hypohidrosis, hypotrichosis, and prominent milia.
Topics: Acneiform Eruptions; Adult; Carcinoma, Basal Cell; Female; Humans; Hypohidrosis; Hypotrichosis; Neop | 2000 |
3 trials available for salicylic acid and Hypotrichosis
| Article | Year |
|---|---|
Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin.
Topics: Gentamicins; Glycoproteins; Humans; Hypotrichosis; Intercellular Signaling Peptides and Proteins; Pe | 2020 |
Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by LIPH Pathogenic Variants.
Topics: Administration, Topical; Adolescent; Child; Child, Preschool; Female; Hair; Hair Diseases; Hair Foll | 2020 |
The Effect of Platelet-Rich Plasma in Hair Regrowth: A Randomized Placebo-Controlled Trial.
Topics: Adult; Follow-Up Studies; Hair Follicle; Humans; Hypotrichosis; Male; Middle Aged; Platelet-Rich Pla | 2015 |
The Effect of Platelet-Rich Plasma in Hair Regrowth: A Randomized Placebo-Controlled Trial.
Topics: Adult; Follow-Up Studies; Hair Follicle; Humans; Hypotrichosis; Male; Middle Aged; Platelet-Rich Pla | 2015 |
The Effect of Platelet-Rich Plasma in Hair Regrowth: A Randomized Placebo-Controlled Trial.
Topics: Adult; Follow-Up Studies; Hair Follicle; Humans; Hypotrichosis; Male; Middle Aged; Platelet-Rich Pla | 2015 |
The Effect of Platelet-Rich Plasma in Hair Regrowth: A Randomized Placebo-Controlled Trial.
Topics: Adult; Follow-Up Studies; Hair Follicle; Humans; Hypotrichosis; Male; Middle Aged; Platelet-Rich Pla | 2015 |
33 other studies available for salicylic acid and Hypotrichosis
| Article | Year |
|---|---|
Hypotrichosis simplex of the scalp and peeling skin disease, two sides of the same coin.
Topics: Humans; Hypotrichosis; Pedigree; Scalp; Skin Abnormalities; Skin Diseases | 2022 |
Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors.
Topics: Alopecia; Humans; Hypotrichosis; Intercellular Signaling Peptides and Proteins; Minoxidil; Scalp | 2022 |
Familial hypotrichosis simplex of the scalp associated with a novel heterozygous nonsense variant in CDSN.
Topics: Codon, Nonsense; Humans; Hypotrichosis; Intercellular Signaling Peptides and Proteins; Pedigree; Sca | 2023 |
Hypotrichosis and Hair Loss on the Occipital Scalp.
Topics: Alopecia; Hair; Humans; Hypotrichosis; Pedigree; Scalp | 2023 |
Reading through genetic 'stop signs': a therapeutic strategy in genetic skin disease.
Topics: Gentamicins; Humans; Hypotrichosis; Reading; Scalp; Skin Diseases, Genetic | 2020 |
Hereditary hypotrichosis simplex of the scalp.
Topics: Alopecia; Child; Diagnosis, Differential; Female; Humans; Hypotrichosis; Pedigree; Scalp | 2017 |
A novel insertion mutation of CDSN responsible for hypotrichosis simplex of scalp in a Chinese family.
Topics: Alopecia; China; Genetic Variation; Glycoproteins; Humans; Hypotrichosis; Intercellular Signaling Pe | 2018 |
Homozygous missense mutation in the LIPH gene causing autosomal recessive hypotrichosis simplex in a Chinese patient.
Topics: Alopecia; Asian People; Child; China; Homozygote; Humans; Hypotrichosis; Lipase; Male; Mutation, Mis | 2014 |
Occipital neuralgia after scalp biopsy and curettage.
Topics: Biopsy; Curettage; Female; Headache Disorders; Humans; Hypotrichosis; Middle Aged; Neuralgia; Scalp; | 2015 |
Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
Topics: Chromosome Mapping; Genes, Recessive; Genotype; Hair; Humans; Hypotrichosis; Male; Middle Aged; Pedi | 2009 |
APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex.
Topics: Animals; beta Catenin; Cell Differentiation; Cell Line; Cell Proliferation; Chick Embryo; Chromosome | 2010 |
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
Topics: Aged; Amyloidosis; Cells, Cultured; Circular Dichroism; Glycoproteins; Humans; Hypotrichosis; In Vit | 2010 |
A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.
Topics: Adolescent; Amino Acid Substitution; DNA Mutational Analysis; Female; Genotype; Humans; Hypotrichosi | 2011 |
[Clinical investigation of a Chinese family with hypotrichosis simplex of the scalp and mutational analysis of CDSN gene].
Topics: Alopecia; China; Codon, Nonsense; Female; Glycoproteins; Humans; Hypotrichosis; Intercellular Signal | 2012 |
Homozygosity mapping of a locus for a novel syndromic ichthyosis to chromosome 3q27-q28.
Topics: Adolescent; Child; Child, Preschool; Cholangitis, Sclerosing; Chromosome Mapping; Chromosomes, Human | 2002 |
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.
Topics: Base Sequence; Child; Chromosomes, Human, Pair 6; Codon, Nonsense; DNA; Genetic Linkage; Glycoprotei | 2003 |
Progressive patterned scalp hypotrichosis, with wiry hair, onycholysis, and intermittently associated cleft lip and palate: clinical and genetic distinction from Marie Unna.
Topics: Adolescent; Adult; Cleft Lip; Cleft Palate; Diagnosis, Differential; Female; Hair; Humans; Hypotrich | 2003 |
Chronic telogen effluvium: a study of 5 patients over 7 years.
Topics: Adolescent; Adult; Alopecia; Biopsy; Chronic Disease; Diagnosis, Differential; Female; Follow-Up Stu | 2005 |
Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions.
Topics: Amino Acid Sequence; Child, Preschool; Desmogleins; DNA Mutational Analysis; Female; Hair; Hair Dise | 2006 |
Hypotrichosis simplex of the scalp.
Topics: Chromosomes, Human, Pair 6; Genes, Dominant; Hair Follicle; Humans; Hypotrichosis; Male; Pedigree; S | 2007 |
[Alopecia areata and diffuse hypotrichosis associated with Ullrich-Turner syndrome. Presentation of 4 patients].
Topics: Adult; Alopecia Areata; Female; Hair; Humans; Hypotrichosis; Scalp; Turner Syndrome | 1993 |
Hereditary hypotrichosis simplex of the scalp.
Topics: Adolescent; Biopsy; Female; Genes, Dominant; Hair; Humans; Hypotrichosis; Microscopy, Electron, Scan | 1995 |
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.
Topics: Adolescent; Age of Onset; Chromosome Mapping; Chromosomes, Human, Pair 6; Female; Genes, Dominant; H | 2000 |
Almost complete absence of the scalp and body hair in association with oligodontia and zygodactylous palmar triradii.
Topics: Abnormalities, Multiple; Adolescent; Dermatoglyphics; Ectodermal Dysplasia; Eyebrows; Eyelashes; Fam | 2001 |
[Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
Topics: Adolescent; Alopecia; Chromosome Aberrations; Chromosome Disorders; Genes, Dominant; Hair; Humans; H | 1979 |
[A case of congenital hypotrichosis with hair abnormalities, scar-like changes of the scalp, corneal changes and a congenital heart defect].
Topics: Abnormalities, Multiple; Alopecia; Child, Preschool; Female; Hair; Heart Defects, Congenital; Humans | 1978 |
Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
Topics: Adult; Age Factors; Aged; Aged, 80 and over; Biopsy; Child; Female; Genes, Dominant; Hair; Humans; H | 1991 |
Hereditary hypotrichosis of the scalp.
Topics: Adult; Child, Preschool; Female; Genes, Dominant; Hair; Humans; Hypotrichosis; Male; Microscopy, Ele | 1991 |
Focal naevoid hypotrichosis.
Topics: Alopecia; Child, Preschool; Humans; Hypotrichosis; Male; Nevus, Pigmented; Scalp; Skin Neoplasms | 1987 |
Hypotrichosis with keratosis pilaris: electrophoretical study of hair fibrous proteins from a patient.
Topics: Adult; Alopecia; Amino Acids; Darier Disease; Electrophoresis, Gel, Two-Dimensional; Hair; Humans; H | 1989 |
Hereditary hypotrichosis simplex of the scalp.
Topics: Adult; Alopecia; Child; Female; Genes, Dominant; Humans; Hypotrichosis; Israel; Jews; Male; Pedigree | 1987 |
[Hypotrichosis congenita hereditaria Maria Unna].
Topics: Adult; Alopecia; Child, Preschool; Female; Hair; Humans; Hypotrichosis; Microscopy, Electron, Scanni | 1985 |
Hereditary hypotrichosis simplex of the scalp. Evidence for autosomal dominant inheritance.
Topics: Adolescent; Adult; Age Factors; Alopecia; Child; Child, Preschool; Chromatography; Female; Genes, Do | 1974 |