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

Year Number of Results
1833 1
1894 1
1896 1
1903 1
1904 1
1908 1
1909 1
1911 1
1912 2
1914 4
1915 7
1918 4
1920 3
1921 1
1922 3
1924 6
1925 7
1926 4
1927 2
1928 6
1929 4
1930 10
1931 7
1932 12
1933 7
1934 7
1935 5
1936 2
1937 3
1938 6
1939 7
1940 10
1941 6
1942 5
1943 4
1944 3
1945 12
1946 58
1947 57
1948 39
1949 38
1950 85
1951 89
1952 97
1953 101
1954 93
1955 97
1956 85
1957 102
1958 100
1959 102
1960 99
1961 102
1962 111
1963 126
1964 151
1965 226
1966 164
1967 183
1968 213
1969 232
1970 247
1971 253
1972 249
1973 237
1974 196
1975 564
1976 602
1977 478
1978 478
1979 391
1980 429
1981 440
1982 463
1983 487
1984 505
1985 498
1986 455
1987 471
1988 457
1989 544
1990 519
1991 493
1992 514
1993 492
1994 430
1995 443
1996 435
1997 410
1998 424
1999 461
2000 516
2001 509
2002 478
2003 575
2004 652
2005 724
2006 797
2007 802
2008 832
2009 927
2010 946
2011 1109
2012 1186
2013 1235
2014 1385
2015 1340
2016 1430
2017 1321
2018 1336
2019 1369
2020 1559
2021 1626
2022 1627
2023 1600
2024 583

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Page 1
Showing results for albino
Your search for alginox retrieved no results
Albinism: epidemiology, genetics, cutaneous characterization, psychosocial factors.
Marçon CR, Maia M. Marçon CR, et al. An Bras Dermatol. 2019 Sep-Oct;94(5):503-520. doi: 10.1016/j.abd.2019.09.023. Epub 2019 Sep 30. An Bras Dermatol. 2019. PMID: 31777350 Free PMC article. Review.
Oculocutaneous albinism is an autosomal recessive disease caused by the complete absence or decrease of melanin biosynthesis in melanocytes. ...In Brazil, as in other parts of the world, albinism remains a little known disorder, both in relation to epidemiological d …
Oculocutaneous albinism is an autosomal recessive disease caused by the complete absence or decrease of melanin biosynthesis in melan …
Molecular characterization of a series of 990 index patients with albinism.
Lasseaux E, Plaisant C, Michaud V, Pennamen P, Trimouille A, Gaston L, Monfermé S, Lacombe D, Rooryck C, Morice-Picard F, Arveiler B. Lasseaux E, et al. Pigment Cell Melanoma Res. 2018 Jul;31(4):466-474. doi: 10.1111/pcmr.12688. Epub 2018 Feb 14. Pigment Cell Melanoma Res. 2018. PMID: 29345414
Albinism is a clinically and genetically heterogeneous disease characterized by variable degrees of hypopigmentation and by nystagmus, foveal hypoplasia, and chiasmatic misrouting of the optic nerves. The wide phenotypic heterogeneity impedes the establishment of phenotype …
Albinism is a clinically and genetically heterogeneous disease characterized by variable degrees of hypopigmentation and by nystagmus …
Albinism.
Witkop CJ Jr. Witkop CJ Jr. Clin Dermatol. 1989 Apr-Jun;7(2):80-91. doi: 10.1016/0738-081x(89)90059-x. Clin Dermatol. 1989. PMID: 2667743 Review. No abstract available.
Primary cutaneous malignancies in nonalbino and albino Africans.
Okafor OC, Onyishi NT. Okafor OC, et al. Int J Dermatol. 2021 Feb;60(2):222-228. doi: 10.1111/ijd.15312. Epub 2020 Nov 28. Int J Dermatol. 2021. PMID: 33247861
Squamous cell carcinoma was the most common type of skin cancer in the albino and nonalbino patients. No case of malignant melanoma was diagnosed in the albino group. CONCLUSION: Albino skin cancer patients were much younger than nonalbinos. Albinos an …
Squamous cell carcinoma was the most common type of skin cancer in the albino and nonalbino patients. No case of malignant melanoma w …
Albinism.
King RA, Summers CG. King RA, et al. Dermatol Clin. 1988 Apr;6(2):217-28. Dermatol Clin. 1988. PMID: 3288382 Review.
Genetic abnormalities of the melanin pigment system in which the synthesis of melanin is reduced or absent are called albinism. The reduction in melanin synthesis can involve the skin, hair follicle, and eye, resulting in oculocutaneous albinism, or can be localized …
Genetic abnormalities of the melanin pigment system in which the synthesis of melanin is reduced or absent are called albinism. The r …
Albinism.
François J. François J. Ophthalmologica. 1979;178(1-2):19-31. doi: 10.1159/000308802. Ophthalmologica. 1979. PMID: 108645 Review.
There are seven forms of oculo-cutaneous albinism, which are all autosomal recessive: three are tyrosinase-negative (complete oculo-cutaneous albinism, Amish albinism, Hermansky-Pudlak syndrome) and four are tyrosinase-positive (incomplete oculo-cutaneous …
There are seven forms of oculo-cutaneous albinism, which are all autosomal recessive: three are tyrosinase-negative (complete oculo-c …
Generation of Albino Phenotype in Ornamental Fish by CRISPR/Cas9-Mediated Genome Editing of slc45a2 Gene.
Zhang C, Ren Z, Gong Z. Zhang C, et al. Mar Biotechnol (NY). 2023 Apr;25(2):281-290. doi: 10.1007/s10126-023-10204-9. Epub 2023 Mar 14. Mar Biotechnol (NY). 2023. PMID: 36917276
Albinism is the most common color variation described in fish and is a fascinating trait of some ornamental fish species. Albino mutants can be generated by knocking out core genes affecting melanin synthesis like slc45a2 in several fish species. ...
Albinism is the most common color variation described in fish and is a fascinating trait of some ornamental fish species. Albino …
Noah; an albino.
SORSBY A. SORSBY A. Br Med J. 1958 Dec 27;2(5112):1587-9. doi: 10.1136/bmj.2.5112.1587. Br Med J. 1958. PMID: 13608062 Free PMC article. No abstract available.
Impaired Direction Selectivity in the Nucleus of the Optic Tract of Albino Mice.
Montijn JS, Riguccini V, Levelt CN, Heimel JA. Montijn JS, et al. Invest Ophthalmol Vis Sci. 2023 Aug 1;64(11):9. doi: 10.1167/iovs.64.11.9. Invest Ophthalmol Vis Sci. 2023. PMID: 37548962 Free PMC article.
METHODS: We recorded neuronal spiking activity with Neuropixels probes in the visual cortex and NOT in C57BL/6JRj mice (pigmented) and DBA/1JRj mice with oculocutaneous albinism (albino). RESULTS: We found that in pigmented mice, NOT is retinotopically organized, an …
METHODS: We recorded neuronal spiking activity with Neuropixels probes in the visual cortex and NOT in C57BL/6JRj mice (pigmented) and DBA/1 …
Oculocutaneous albinism.
Okulicz JF, Shah RS, Schwartz RA, Janniger CK. Okulicz JF, et al. J Eur Acad Dermatol Venereol. 2003 May;17(3):251-6. doi: 10.1046/j.1468-3083.2003.00767.x. J Eur Acad Dermatol Venereol. 2003. PMID: 12702061 Review.
Oculocutaneous albinism represents a group of inherited skin disorders characterized by a generalized reduction of cutaneous, ocular and pilar pigmentation from the time of birth. Oculocutaneous albinism types 1 and 2 are the most common, but several other types hav …
Oculocutaneous albinism represents a group of inherited skin disorders characterized by a generalized reduction of cutaneous, ocular …
39,122 results
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