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

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1993 1
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12 results

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Page 1
The role of vitamin D in melanogenesis with an emphasis on vitiligo.
AlGhamdi K, Kumar A, Moussa N. AlGhamdi K, et al. Indian J Dermatol Venereol Leprol. 2013 Nov-Dec;79(6):750-8. doi: 10.4103/0378-6323.120720. Indian J Dermatol Venereol Leprol. 2013. PMID: 24177606 Free article. Review.
Our review revealed that vitamin D deficiency has been identified in many conditions, including premature and dysmature birth, pigmented skin, obesity, advanced age, and malabsorption. Vitamin D increases melanogenesis and the tyrosinase content of cultured human melanocyt …
Our review revealed that vitamin D deficiency has been identified in many conditions, including premature and dysmature birth, pigmented ski …
Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
Nicholls RD. Nicholls RD. Am J Med Genet. 1993 Apr 1;46(1):16-25. doi: 10.1002/ajmg.1320460106. Am J Med Genet. 1993. PMID: 8388169 Review.
Here, I review the role of uniparental disomy and genomic imprinting in the pathogenesis of AS and PWS, and briefly discuss phenotype-genotype correlations using candidate genes and mouse models, in particular for hypopigmentation....
Here, I review the role of uniparental disomy and genomic imprinting in the pathogenesis of AS and PWS, and briefly discuss phenotype-genoty …
Prader-Willi syndrome and Angelman syndrome: Visualisation of the molecular pathways for two chromosomal disorders.
Ehrhart F, Janssen KJM, Coort SL, Evelo CT, Curfs LMG. Ehrhart F, et al. World J Biol Psychiatry. 2019 Nov;20(9):670-682. doi: 10.1080/15622975.2018.1439594. Epub 2018 Mar 1. World J Biol Psychiatry. 2019. PMID: 29425059 Review.
Patients of both disorders exhibit hypotonia in neonatal stage, delay in development and hypopigmentation. Typical features for PWS include hyperphagia, which leads to obesity, the major cause of mortality, and hypogonadism. ...
Patients of both disorders exhibit hypotonia in neonatal stage, delay in development and hypopigmentation. Typical features for PWS i …
Avian models with spontaneous autoimmune diseases.
Wick G, Andersson L, Hala K, Gershwin ME, Selmi C, Erf GF, Lamont SJ, Sgonc R. Wick G, et al. Adv Immunol. 2006;92:71-117. doi: 10.1016/S0065-2776(06)92002-1. Adv Immunol. 2006. PMID: 17145302 Free PMC article. Review.
The present chapter describes three spontaneous chicken models for human autoimmune diseases, the Obese strain (OS) with a Hashimoto-like autoimmune thyroiditis, the University of California at Davis lines 200 and 206 (UCD-200 and -206) with a scleroderma-like disease, and …
The present chapter describes three spontaneous chicken models for human autoimmune diseases, the Obese strain (OS) with a Hashimoto- …
The mouse p (pink-eyed dilution) and human P genes, oculocutaneous albinism type 2 (OCA2), and melanosomal pH.
Brilliant MH. Brilliant MH. Pigment Cell Res. 2001 Apr;14(2):86-93. doi: 10.1034/j.1600-0749.2001.140203.x. Pigment Cell Res. 2001. PMID: 11310796 Review.
Recessive mutations of the mouse p (pink-eyed dilution) gene lead to hypopigmentation of the eyes, skin, and fur. Mice lacking a functional p protein have pink eyes and light gray fur (if non-agouti) or cream-colored fur (if agouti). ...
Recessive mutations of the mouse p (pink-eyed dilution) gene lead to hypopigmentation of the eyes, skin, and fur. Mice lacking a func …
Albinism: modern molecular diagnosis.
Carden SM, Boissy RE, Schoettker PJ, Good WV. Carden SM, et al. Br J Ophthalmol. 1998 Feb;82(2):189-95. doi: 10.1136/bjo.82.2.189. Br J Ophthalmol. 1998. PMID: 9613388 Free PMC article. Review. No abstract available.
[Diploid/triploid mosaicism: a variable but characteristic phenotype].
Natera-De Benito D, Poo P, Gean E, Vicente-Villa A, García-Cazorla A, Fons-Estupiña MC. Natera-De Benito D, et al. Rev Neurol. 2014 Aug 16;59(4):158-63. Rev Neurol. 2014. PMID: 25059266 Free article. Review. Spanish.
The most frequently observed symptoms were mental retardation, truncal obesity, short stature, hemihypertrophy, small and narrow hands with clino and camptodactyly. ...CONCLUSIONS: Intellectual disability associated with truncal obesity, short stature, hemihypertrop …
The most frequently observed symptoms were mental retardation, truncal obesity, short stature, hemihypertrophy, small and narrow hand …
Common hyperpigmentation disorders in adults: Part II. Melanoma, seborrheic keratoses, acanthosis nigricans, melasma, diabetic dermopathy, tinea versicolor, and postinflammatory hyperpigmentation.
Stulberg DL, Clark N, Tovey D. Stulberg DL, et al. Am Fam Physician. 2003 Nov 15;68(10):1963-8. Am Fam Physician. 2003. PMID: 14655805 Free article. Review.
., gastrointestinal tumor), it more often is associated with insulin resistance (type 2 diabetes, polycystic ovary syndrome) or obesity. Melasma is a facial hyperpigmentation resulting from the stimulation of melanocytes by endogenous or exogenous estrogen. ...Tinea versic …
., gastrointestinal tumor), it more often is associated with insulin resistance (type 2 diabetes, polycystic ovary syndrome) or obesity …
Bier spots are an under-recognized cutaneous manifestation of lower extremity lymphedema: a case series and brief review of the literature.
Dean SM, Zirwas M. Dean SM, et al. Ann Vasc Surg. 2014 Nov;28(8):1935.e13-6. doi: 10.1016/j.avsg.2014.07.005. Epub 2014 Jul 10. Ann Vasc Surg. 2014. PMID: 25017780 Review.
Eleven patients between 23 and 70 years of age (5 male and 6 female) were diagnosed with Bier spots as evidenced by reversible white macules ranging from 3 to 8 mm in diameter on the extensor portions of the feet, ankles, and calves. The thighs were affected as well in 2 morbidly …
Eleven patients between 23 and 70 years of age (5 male and 6 female) were diagnosed with Bier spots as evidenced by reversible white macules …
12 results