Palmoplantar keratoderma (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Palmoplantar keratoderma" in English language version.

refsWebsite

Global rank English rank

20nih.gov

4^th place

15doi.org

2^nd place

6semanticscholar.org

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2omim.org

4,380^th place

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1cdlib.org

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1whonamedit.com

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cdlib.org

dermatology.cdlib.org

Leonard AL, Freedberg IM (October 2003). "Palmoplantar keratoderma of Sybert". Dermatology Online Journal. 9 (4): 30. doi:10.5070/D31QG46424. PMID 14594603.

doi.org

Patel S, Zirwas M, English JC (2007). "Acquired palmoplantar keratoderma". American Journal of Clinical Dermatology. 8 (1): 1–11. doi:10.2165/00128071-200708010-00001. PMID 17298101. S2CID 7221815.
Ryan P, Baird G, Benfanti P (March 2007). "Hereditary painful callosities: case report and review of the literature". Foot & Ankle International. 28 (3): 377–8. doi:10.3113/FAI.2007.0377. PMID 17371662. S2CID 10787216.
Martinez-Mir A, Zlotogorski A, Londono D, Gordon D, Grunn A, Uribe E, Horev L, Ruiz IM, Davalos NO, Alayan O, Liu J, Gilliam TC, Salas-Alanis JC, Christiano AM (December 2003). "Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24". Journal of Medical Genetics. 40 (12): 872–8. doi:10.1136/jmg.40.12.872. PMC 1735333. PMID 14684683.
Erkek E, Koçak M, Bozdoğan O, Atasoy P, Birol A (2004). "Focal acral hyperkeratosis: a rare cutaneous disorder within the spectrum of Costa acrokeratoelastoidosis". Pediatric Dermatology. 21 (2): 128–30. doi:10.1111/j.0736-8046.2004.21208.x. PMID 15078352. S2CID 19811383.
Leonard AL, Freedberg IM (October 2003). "Palmoplantar keratoderma of Sybert". Dermatology Online Journal. 9 (4): 30. doi:10.5070/D31QG46424. PMID 14594603.
Gach JE, Munro CS, Lane EB, Wilson NJ, Moss C (November 2005). "Two families with Greither's syndrome caused by a keratin 1 mutation". Journal of the American Academy of Dermatology. 53 (5 Suppl 1): S225-30. doi:10.1016/j.jaad.2005.01.139. PMID 16227096.
Sybert VP, Dale BA, Holbrook KA (January 1988). "Palmar-plantar keratoderma. A clinical, ultrastructural, and biochemical study". Journal of the American Academy of Dermatology. 18 (1 Pt 1): 75–86. doi:10.1016/S0190-9622(88)70012-2. PMID 2450111.
Lee YA, Stevens HP, Delaporte E, Wahn U, Reis A (January 2000). "A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23". American Journal of Human Genetics. 66 (1): 326–30. doi:10.1086/302718. PMC 1288338. PMID 10631162.
Maestrini E, Korge BP, Ocaña-Sierra J, Calzolari E, Cambiaghi S, Scudder PM, Hovnanian A, Monaco AP, Munro CS (July 1999). "A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families". Human Molecular Genetics. 8 (7): 1237–43. doi:10.1093/hmg/8.7.1237. PMID 10369869.
Vohwinkel KH (1929). "Keratoma hereditarium mutilans". Archiv für Dermatologie und Syphilis. 158 (2): 354–364. doi:10.1007/bf01826619. S2CID 1737564.
Kumar P, Sharma PK, Kar HK (2008). "Olmsted syndrome". Indian Journal of Dermatology. 53 (2): 93–5. doi:10.4103/0019-5154.41657. PMC 2763718. PMID 19881998.
Dessureault J, Poulin Y, Bourcier M, Gagne E (2003). "Olmsted syndrome-palmoplantar and periorificial keratodermas: association with malignant melanoma". Journal of Cutaneous Medicine and Surgery. 7 (3): 236–42. doi:10.1007/s10227-002-0107-4. PMID 12704531. S2CID 23612959.
Lin Z, Chen Q, Lee M, Cao X, Zhang J, Ma D, Chen L, Hu X, Wang H, Wang X, Zhang P, Liu X, Guan L, Tang Y, Yang H, Tu P, Bu D, Zhu X, Wang K, Li R, Yang Y (March 2012). "Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome". American Journal of Human Genetics. 90 (3): 558–64. doi:10.1016/j.ajhg.2012.02.006. PMC 3309189. PMID 22405088.
Garçon-Michel N, Roguedas-Contios AM, Rault G, Le Bihan J, Ramel S, Revert K, Dirou A, Misery L (July 2010). "Frequency of aquagenic palmoplantar keratoderma in cystic fibrosis: a new sign of cystic fibrosis?". The British Journal of Dermatology. 163 (1): 162–6. doi:10.1111/j.1365-2133.2010.09764.x. PMID 20302572. S2CID 26018635.
Sezer E, Durmaz EÖ, Çetin E, Şahin S (2015). "Permanent treatment of aquagenic syringeal acrokeratoderma with endoscopic thoracic sympathectomy". Indian Journal of Dermatology, Venereology and Leprology. 81 (6): 648–50. doi:10.4103/0378-6323.168331. PMID 26515860.

nih.gov

pubmed.ncbi.nlm.nih.gov

Patel S, Zirwas M, English JC (2007). "Acquired palmoplantar keratoderma". American Journal of Clinical Dermatology. 8 (1): 1–11. doi:10.2165/00128071-200708010-00001. PMID 17298101. S2CID 7221815.
Ryan P, Baird G, Benfanti P (March 2007). "Hereditary painful callosities: case report and review of the literature". Foot & Ankle International. 28 (3): 377–8. doi:10.3113/FAI.2007.0377. PMID 17371662. S2CID 10787216.
Martinez-Mir A, Zlotogorski A, Londono D, Gordon D, Grunn A, Uribe E, Horev L, Ruiz IM, Davalos NO, Alayan O, Liu J, Gilliam TC, Salas-Alanis JC, Christiano AM (December 2003). "Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24". Journal of Medical Genetics. 40 (12): 872–8. doi:10.1136/jmg.40.12.872. PMC 1735333. PMID 14684683.
Erkek E, Koçak M, Bozdoğan O, Atasoy P, Birol A (2004). "Focal acral hyperkeratosis: a rare cutaneous disorder within the spectrum of Costa acrokeratoelastoidosis". Pediatric Dermatology. 21 (2): 128–30. doi:10.1111/j.0736-8046.2004.21208.x. PMID 15078352. S2CID 19811383.
Leonard AL, Freedberg IM (October 2003). "Palmoplantar keratoderma of Sybert". Dermatology Online Journal. 9 (4): 30. doi:10.5070/D31QG46424. PMID 14594603.
Greither A (May 1952). "[Keratosis extremitatum hereditaria progrediens with genetic dominant]". Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und Verwandte Gebiete. 3 (5): 198–203. PMID 14945735.
Gach JE, Munro CS, Lane EB, Wilson NJ, Moss C (November 2005). "Two families with Greither's syndrome caused by a keratin 1 mutation". Journal of the American Academy of Dermatology. 53 (5 Suppl 1): S225-30. doi:10.1016/j.jaad.2005.01.139. PMID 16227096.
Sybert VP, Dale BA, Holbrook KA (January 1988). "Palmar-plantar keratoderma. A clinical, ultrastructural, and biochemical study". Journal of the American Academy of Dermatology. 18 (1 Pt 1): 75–86. doi:10.1016/S0190-9622(88)70012-2. PMID 2450111.
Lee YA, Stevens HP, Delaporte E, Wahn U, Reis A (January 2000). "A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23". American Journal of Human Genetics. 66 (1): 326–30. doi:10.1086/302718. PMC 1288338. PMID 10631162.
Huriez C, Deminatti M, Agache P, Mennecier M (February 1968). "[A gene dysplasia not previously known: frequently degenerative sclero-atrophying and keratodermic genodermatosis of the extremities]". La Semaine des Hopitaux (in French). 44 (8): 481–8. PMID 4298032.
Maestrini E, Korge BP, Ocaña-Sierra J, Calzolari E, Cambiaghi S, Scudder PM, Hovnanian A, Monaco AP, Munro CS (July 1999). "A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families". Human Molecular Genetics. 8 (7): 1237–43. doi:10.1093/hmg/8.7.1237. PMID 10369869.
Kumar P, Sharma PK, Kar HK (2008). "Olmsted syndrome". Indian Journal of Dermatology. 53 (2): 93–5. doi:10.4103/0019-5154.41657. PMC 2763718. PMID 19881998.
Dessureault J, Poulin Y, Bourcier M, Gagne E (2003). "Olmsted syndrome-palmoplantar and periorificial keratodermas: association with malignant melanoma". Journal of Cutaneous Medicine and Surgery. 7 (3): 236–42. doi:10.1007/s10227-002-0107-4. PMID 12704531. S2CID 23612959.
Lin Z, Chen Q, Lee M, Cao X, Zhang J, Ma D, Chen L, Hu X, Wang H, Wang X, Zhang P, Liu X, Guan L, Tang Y, Yang H, Tu P, Bu D, Zhu X, Wang K, Li R, Yang Y (March 2012). "Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome". American Journal of Human Genetics. 90 (3): 558–64. doi:10.1016/j.ajhg.2012.02.006. PMC 3309189. PMID 22405088.
Garçon-Michel N, Roguedas-Contios AM, Rault G, Le Bihan J, Ramel S, Revert K, Dirou A, Misery L (July 2010). "Frequency of aquagenic palmoplantar keratoderma in cystic fibrosis: a new sign of cystic fibrosis?". The British Journal of Dermatology. 163 (1): 162–6. doi:10.1111/j.1365-2133.2010.09764.x. PMID 20302572. S2CID 26018635.
Sezer E, Durmaz EÖ, Çetin E, Şahin S (2015). "Permanent treatment of aquagenic syringeal acrokeratoderma with endoscopic thoracic sympathectomy". Indian Journal of Dermatology, Venereology and Leprology. 81 (6): 648–50. doi:10.4103/0378-6323.168331. PMID 26515860.

ncbi.nlm.nih.gov

Martinez-Mir A, Zlotogorski A, Londono D, Gordon D, Grunn A, Uribe E, Horev L, Ruiz IM, Davalos NO, Alayan O, Liu J, Gilliam TC, Salas-Alanis JC, Christiano AM (December 2003). "Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24". Journal of Medical Genetics. 40 (12): 872–8. doi:10.1136/jmg.40.12.872. PMC 1735333. PMID 14684683.
Lee YA, Stevens HP, Delaporte E, Wahn U, Reis A (January 2000). "A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23". American Journal of Human Genetics. 66 (1): 326–30. doi:10.1086/302718. PMC 1288338. PMID 10631162.
Kumar P, Sharma PK, Kar HK (2008). "Olmsted syndrome". Indian Journal of Dermatology. 53 (2): 93–5. doi:10.4103/0019-5154.41657. PMC 2763718. PMID 19881998.
Lin Z, Chen Q, Lee M, Cao X, Zhang J, Ma D, Chen L, Hu X, Wang H, Wang X, Zhang P, Liu X, Guan L, Tang Y, Yang H, Tu P, Bu D, Zhu X, Wang K, Li R, Yang Y (March 2012). "Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome". American Journal of Human Genetics. 90 (3): 558–64. doi:10.1016/j.ajhg.2012.02.006. PMC 3309189. PMID 22405088.

omim.org

Online Mendelian Inheritance in Man (OMIM): 144200
Online Mendelian Inheritance in Man (OMIM): 600962

semanticscholar.org

api.semanticscholar.org

Patel S, Zirwas M, English JC (2007). "Acquired palmoplantar keratoderma". American Journal of Clinical Dermatology. 8 (1): 1–11. doi:10.2165/00128071-200708010-00001. PMID 17298101. S2CID 7221815.
Ryan P, Baird G, Benfanti P (March 2007). "Hereditary painful callosities: case report and review of the literature". Foot & Ankle International. 28 (3): 377–8. doi:10.3113/FAI.2007.0377. PMID 17371662. S2CID 10787216.
Erkek E, Koçak M, Bozdoğan O, Atasoy P, Birol A (2004). "Focal acral hyperkeratosis: a rare cutaneous disorder within the spectrum of Costa acrokeratoelastoidosis". Pediatric Dermatology. 21 (2): 128–30. doi:10.1111/j.0736-8046.2004.21208.x. PMID 15078352. S2CID 19811383.
Vohwinkel KH (1929). "Keratoma hereditarium mutilans". Archiv für Dermatologie und Syphilis. 158 (2): 354–364. doi:10.1007/bf01826619. S2CID 1737564.
Dessureault J, Poulin Y, Bourcier M, Gagne E (2003). "Olmsted syndrome-palmoplantar and periorificial keratodermas: association with malignant melanoma". Journal of Cutaneous Medicine and Surgery. 7 (3): 236–42. doi:10.1007/s10227-002-0107-4. PMID 12704531. S2CID 23612959.
Garçon-Michel N, Roguedas-Contios AM, Rault G, Le Bihan J, Ramel S, Revert K, Dirou A, Misery L (July 2010). "Frequency of aquagenic palmoplantar keratoderma in cystic fibrosis: a new sign of cystic fibrosis?". The British Journal of Dermatology. 163 (1): 162–6. doi:10.1111/j.1365-2133.2010.09764.x. PMID 20302572. S2CID 26018635.

whonamedit.com

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