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research Acrodermatitis continua resistant to etanercept: Therapeutic challenge and Unfortunate outcome

6 citations , June 2008 in “Journal of the European Academy of Dermatology and Venereology”

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

research Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II

18 citations , November 2009 in “Calcified tissue international”

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

research Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh

January 2017 in “IMC Journal of Medical Science”

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

research Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain

6 citations , November 2011 in “Journal of Dermatological Science”

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

research Late onset nevus comedonicus of scalp: a rare site for an uncommon condition

1 citations , January 2019 in “Dermatology Online Journal”

A rare skin condition appeared on a 19-year-old woman's scalp.

research More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players

35 citations , May 2006 in “Journal of Investigative Dermatology”

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

research [P233] A case of acquired trichorrhexis nodosa with iron deficiency anemia

January 2017 in “프로그램북(구 초록집)”

Iron deficiency anemia can cause hair breakage.

research Comparative Anatomy of Mouse and Human Nail Units

55 citations , February 2013 in “The Anatomical Record”

Mouse nails are similar to human nails, making them useful for studying nail diseases.

research Moniletherix

January 2013 in “The Pan African medical journal”

Monilethrix causes short, fragile hair with no specific treatment available.

research Monilethrix: the use of tricoscopy in clinical diagnosis

1 citations , June 2016 in “Medicina”

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

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