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Table representation of search results timeline featuring number of search results per year.

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2007 1
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Quoted phrase not found in phrase index: "Regional abnormality of skin"
Page 1
Comorbidities in alopecia areata: A systematic review and meta-analysis.
Lee S, Lee H, Lee CH, Lee WS. Lee S, et al. J Am Acad Dermatol. 2019 Feb;80(2):466-477.e16. doi: 10.1016/j.jaad.2018.07.013. Epub 2018 Jul 18. J Am Acad Dermatol. 2019. PMID: 30031145
Atopic diseases, metabolic syndrome, Helicobacter pylori infection, lupus erythematosus, iron deficiency anemia, thyroid diseases, psychiatric diseases, vitamin D deficiency, and audiologic and ophthalmic abnormalities were more prevalent in patients with AA. Patients with …
Atopic diseases, metabolic syndrome, Helicobacter pylori infection, lupus erythematosus, iron deficiency anemia, thyroid diseases, psychiatr …
Management of hypertrophic scars in adults: A systematic review and meta-analysis.
Choi C, Mukovozov I, Jazdarehee A, Rai R, Sachdeva M, Shunmugam M, Zaslavsky K, Byun S, Barankin B. Choi C, et al. Australas J Dermatol. 2022 May;63(2):172-189. doi: 10.1111/ajd.13790. Epub 2022 Jan 31. Australas J Dermatol. 2022. PMID: 35099068 Review.
Hypertrophic scars (HTS) are elevated scars which occur due to abnormalities in wound healing after injury and may be associated with pain, pruritus and functional impairment. ...
Hypertrophic scars (HTS) are elevated scars which occur due to abnormalities in wound healing after injury and may be associated with …
Genotypic and phenotypic spectra of hemojuvelin mutations in primary hemochromatosis patients: a systematic review.
Kong X, Xie L, Zhu H, Song L, Xing X, Yang W, Chen X. Kong X, et al. Orphanet J Rare Dis. 2019 Jul 8;14(1):171. doi: 10.1186/s13023-019-1097-2. Orphanet J Rare Dis. 2019. PMID: 31286966 Free PMC article. Review.
Hereditary hemochromatosis (HH) is a genetic disorder that causes excess absorption of iron and can lead to a variety of complications including liver cirrhosis, arthritis, abnormal skin pigmentation, cardiomyopathy, hypogonadism, and diabetes. ...The present review …
Hereditary hemochromatosis (HH) is a genetic disorder that causes excess absorption of iron and can lead to a variety of complications inclu …
Scientific evidence of the therapeutic effects of dead sea treatments: a systematic review.
Katz U, Shoenfeld Y, Zakin V, Sherer Y, Sukenik S. Katz U, et al. Semin Arthritis Rheum. 2012 Oct;42(2):186-200. doi: 10.1016/j.semarthrit.2012.02.006. Epub 2012 Apr 12. Semin Arthritis Rheum. 2012. PMID: 22503590 Review.
In the safety analysis, we found no evidence for an increase in skin neoplasia, although skin actinic damage seems to be increased in patients treated in the Dead Sea. ...Substantial ingestion of Dead Sea water (generally in unusual near-drowning cases) is toxic and …
In the safety analysis, we found no evidence for an increase in skin neoplasia, although skin actinic damage seems to be incre …
Management of Skin Reactions During Cetuximab Treatment in Association With Chemotherapy or Radiotherapy: Update of the Italian Expert Recommendations.
Pinto C, Barone CA, Girolomoni G, Russi EG, Merlano MC, Ferrari D, Maiello E. Pinto C, et al. Am J Clin Oncol. 2016 Aug;39(4):407-15. doi: 10.1097/COC.0000000000000291. Am J Clin Oncol. 2016. PMID: 27077276 Review.
A meeting of the panel was held after the first rating session. RESULTS: Skin reactions included acneiformic rash, skin dryness (xerosis), pruritus, paronychia, hair abnormalities, mucositis, and increased growth of eyelashes or facial hair. ...CONCLUSIONS: T …
A meeting of the panel was held after the first rating session. RESULTS: Skin reactions included acneiformic rash, skin drynes …
Dental approach for Apert syndrome in children: a systematic review.
López-Estudillo AS, Rosales-Bérber MA, Ruiz-Rodríguez S, Pozos-Guillén A, Noyola-Frías MÁ, Garrocho-Rangel A. López-Estudillo AS, et al. Med Oral Patol Oral Cir Bucal. 2017 Nov 1;22(6):e660-e668. doi: 10.4317/medoral.21628. Med Oral Patol Oral Cir Bucal. 2017. PMID: 29053644 Free PMC article. Review.
BACKGROUND: Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis condition resulting from missense mutations in the gene encoding fibroblast growth factor receptor 2. It is characterized by three specific clinical features: brachycep …
BACKGROUND: Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis condition resulting from mis …
Interventions for Old World cutaneous leishmaniasis.
Heras-Mosteiro J, Monge-Maillo B, Pinart M, Lopez Pereira P, Reveiz L, Garcia-Carrasco E, Campuzano Cuadrado P, Royuela A, Mendez Roman I, López-Vélez R. Heras-Mosteiro J, et al. Cochrane Database Syst Rev. 2017 Dec 1;12(12):CD005067. doi: 10.1002/14651858.CD005067.pub5. Cochrane Database Syst Rev. 2017. PMID: 29192424 Free PMC article. Review.
SEARCH METHODS: We updated our searches of the following databases to November 2016: the Cochrane Skin Specialised Register, CENTRAL, MEDLINE, Embase, and LILACS. ...The studies included were conducted mainly in the Far or Middle East at regional hospitals, local he …
SEARCH METHODS: We updated our searches of the following databases to November 2016: the Cochrane Skin Specialised Register, CENTRAL, …
Interventions for Old World cutaneous leishmaniasis.
Heras-Mosteiro J, Monge-Maillo B, Pinart M, Lopez Pereira P, Reveiz L, Garcia-Carrasco E, Campuzano Cuadrado P, Royuela A, Mendez Roman I, López-Vélez R. Heras-Mosteiro J, et al. Cochrane Database Syst Rev. 2017 Nov 17;11(11):CD005067. doi: 10.1002/14651858.CD005067.pub4. Cochrane Database Syst Rev. 2017. Update in: Cochrane Database Syst Rev. 2017 Dec 01;12:CD005067. doi: 10.1002/14651858.CD005067.pub5. PMID: 29149474 Free PMC article. Updated. Review.
SEARCH METHODS: We updated our searches of the following databases to November 2016: the Cochrane Skin Specialised Register, CENTRAL, MEDLINE, Embase, and LILACS. ...The studies included were conducted mainly in the Far or Middle East at regional hospitals, local he …
SEARCH METHODS: We updated our searches of the following databases to November 2016: the Cochrane Skin Specialised Register, CENTRAL, …
Effectiveness of photodynamic therapy for mammary and extra-mammary Paget's disease: a state of the science review.
Nardelli AA, Stafinski T, Menon D. Nardelli AA, et al. BMC Dermatol. 2011 Jun 15;11:13. doi: 10.1186/1471-5945-11-13. BMC Dermatol. 2011. PMID: 21676258 Free PMC article. Review.
BACKGROUND: Paget's disease is a rare skin disorder occurring in the breast (mammary) or in the groin, genital, peri-anal and axillary regions (extra-mammary). ...Follow-up periods were typically one year or less, with 77/133 extra-mammary lesions exhibiting complet …
BACKGROUND: Paget's disease is a rare skin disorder occurring in the breast (mammary) or in the groin, genital, peri-anal and axillar …
19 results