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Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth, and Defects of Bone Marrow and Integument

research Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth, and Defects of Bone Marrow and Integument

80 citations, March 2004 in “Neuropediatrics”

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

research Female Hirsutism: Pathophysiological Considerations and Therapeutic Implications

53 citations, October 1984 in “Endocrine reviews”

Excessive hair growth in women often has no known cause and is not linked to race or other hormonal symptoms.

research Characteristic Localization of Neuronatin in Rat Testis, Hair Follicle, Tongue, and Pancreas

2 citations, March 2019 in “Journal of Histochemistry and Cytochemistry”

Neuronatin is found in specific cells within rat testis, hair follicles, tongue, and pancreas, suggesting it has various roles in tissue development and function.

research Advances in the Treatment of Autosomal Recessive Congenital Ichthyosis: A Look Towards the Repositioning of Drugs

November 2023 in “Frontiers in pharmacology”

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

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