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

Year Number of Results
1945 1
1946 2
1947 2
1950 3
1953 1
1956 1
1958 1
1961 1
1962 2
1963 2
1964 7
1965 3
1966 3
1967 4
1968 13
1969 8
1970 20
1971 18
1972 19
1973 16
1974 32
1975 29
1976 30
1977 27
1978 35
1979 49
1980 43
1981 50
1982 50
1983 64
1984 59
1985 69
1986 70
1987 68
1988 45
1989 67
1990 67
1991 57
1992 58
1993 76
1994 78
1995 83
1996 92
1997 89
1998 83
1999 86
2000 88
2001 102
2002 83
2003 71
2004 90
2005 103
2006 124
2007 135
2008 134
2009 116
2010 132
2011 136
2012 152
2013 190
2014 183
2015 184
2016 161
2017 165
2018 198
2019 171
2020 194
2021 160
2022 148
2023 133
2024 47

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4,683 results

Results by year

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Quoted phrase not found in phrase index: "Abnormality of the integument"
Page 1
Epidermolysis bullosa.
Bardhan A, Bruckner-Tuderman L, Chapple ILC, Fine JD, Harper N, Has C, Magin TM, Marinkovich MP, Marshall JF, McGrath JA, Mellerio JE, Polson R, Heagerty AH. Bardhan A, et al. Nat Rev Dis Primers. 2020 Sep 24;6(1):78. doi: 10.1038/s41572-020-0210-0. Nat Rev Dis Primers. 2020. PMID: 32973163 Review.
Over 30 subtypes are recognized, grouped into four major categories, based predominantly on the plane of cleavage within the skin and reflecting the underlying molecular abnormality: EB simplex, junctional EB, dystrophic EB and Kindler EB. ...
Over 30 subtypes are recognized, grouped into four major categories, based predominantly on the plane of cleavage within the skin and reflec …
Keratosis pilaris: an update and approach to management.
Kodali N, Patel VM, Schwartz RA. Kodali N, et al. Ital J Dermatol Venerol. 2023 Jun;158(3):217-223. doi: 10.23736/S2784-8671.23.07594-1. Epub 2023 May 11. Ital J Dermatol Venerol. 2023. PMID: 37166753 Free article. Review.
Female Androgenetic Alopecia: An Update on Diagnosis and Management.
Starace M, Orlando G, Alessandrini A, Piraccini BM. Starace M, et al. Am J Clin Dermatol. 2020 Feb;21(1):69-84. doi: 10.1007/s40257-019-00479-x. Am J Clin Dermatol. 2020. PMID: 31677111 Review.
The role of androgens is not clearly defined and only one-third of women with FAGA show abnormal androgen levels. Endocrinological diseases with hyperandrogenism associated with FAGA comprise polycystic ovarian syndrome (PCOS), hyperprolactinemia, adrenal hyperplasia and, …
The role of androgens is not clearly defined and only one-third of women with FAGA show abnormal androgen levels. Endocrinological di …
Keratosis pilaris.
Drivenes JL, Vasilescu IC, Bygum A. Drivenes JL, et al. Tidsskr Nor Laegeforen. 2023 Mar 7;143(5). doi: 10.4045/tidsskr.22.0513. Print 2023 Mar 28. Tidsskr Nor Laegeforen. 2023. PMID: 36987905 Free article. English, Norwegian.
Immunobullous disease.
Tull TJ, Benton E. Tull TJ, et al. Clin Med (Lond). 2021 May;21(3):162-165. doi: 10.7861/clinmed.2021-0232. Clin Med (Lond). 2021. PMID: 34001564 Free PMC article.
Skin dimples.
Kumar A, Kanojia RK, Saili A. Kumar A, et al. Int J Dermatol. 2014 Jul;53(7):789-97. doi: 10.1111/ijd.12376. Epub 2014 Apr 16. Int J Dermatol. 2014. PMID: 24738724 Review.
Neurocutaneous syndromes in art and antiquities.
Ruggieri M, Gentile AE, Ferrara V, Papi M, Praticò AD, Mudry A, Taruscio D, Micali G, Polizzi A. Ruggieri M, et al. Am J Med Genet C Semin Med Genet. 2021 Jun;187(2):224-234. doi: 10.1002/ajmg.c.31917. Epub 2021 May 20. Am J Med Genet C Semin Med Genet. 2021. PMID: 34013593 Free PMC article. Review.
Neurocutaneous syndromes are a group of genetic disorders affecting the skin, the central and peripheral nervous system, and the eye with congenital abnormalities and/or tumors. Manifestations may also involve the heart, vessels, lungs, kidneys, endocrine gla …
Neurocutaneous syndromes are a group of genetic disorders affecting the skin, the central and peripheral nervous system, and the eye …
Hereditary Hearing Impairment with Cutaneous Abnormalities.
Lee TL, Lin PH, Chen PL, Hong JB, Wu CC. Lee TL, et al. Genes (Basel). 2020 Dec 30;12(1):43. doi: 10.3390/genes12010043. Genes (Basel). 2020. PMID: 33396879 Free PMC article. Review.
In this article, we performed a comprehensive PubMed database search on syndromic HHI with cutaneous abnormalities, and reviewed a total of 260 relevant publications. Our in-depth analyses revealed that the cutaneous manifestations associated with HHI could be classified i …
In this article, we performed a comprehensive PubMed database search on syndromic HHI with cutaneous abnormalities, and reviewed a to …
Leopard syndrome.
Sarkozy A, Digilio MC, Dallapiccola B. Sarkozy A, et al. Orphanet J Rare Dis. 2008 May 27;3:13. doi: 10.1186/1750-1172-3-13. Orphanet J Rare Dis. 2008. PMID: 18505544 Free PMC article. Review.
LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainly characterized by skin, facial and cardiac anomalies. LEOPARD is an acronym for the major features of this disorder, including multiple Lentigines, ECG conduction abnormalities …
LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainly characterized by skin, facial and cardia …
Hypomelanosis of Ito.
Ream M. Ream M. Handb Clin Neurol. 2015;132:281-9. doi: 10.1016/B978-0-444-62702-5.00021-4. Handb Clin Neurol. 2015. PMID: 26564088 Review.
The neurologic complications can include seizures, hemimegalencephaly, developmental delay and abnormalities in tone. Genetic mosaicism is the most likely explanation for its inheritance. ...
The neurologic complications can include seizures, hemimegalencephaly, developmental delay and abnormalities in tone. Genetic mosaici …
4,683 results