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research Exploring the Role of GLP‐1 Agents in Managing Diabetic Foot Ulcers: A Narrative and Systematic Review

September 2025 in “Wound Repair and Regeneration”

GLP-1 receptor agonists may help manage and prevent diabetic foot ulcers.

research Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat

28 citations , October 2004 in “Differentiation”

A gene deletion causes the "hairless" trait in Iffa Credo rats.

research Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets

29 citations , January 2003 in “KARGER eBooks”

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

research 41761 Alpha-gal Syndrome for the Dermatologist

September 2023 in “Journal of the American Academy of Dermatology”

Dermatologists should consider alpha-gal syndrome in patients with unexplained chronic skin issues.

research Linear Basal Cell Carcinomas

3 citations , May 1999 in “Dermatologic Surgery”

Dr. Connelly agrees that linear basal cell carcinomas might be more aggressive but highlights the study's lack of clear criteria to identify them.

research Treatment options and emotional well-being in patients with rosacea: An unsupervised machine learning analysis of over 200,000 posts

6 citations , July 2023 in “JAAD International”

Rosacea patients often discuss treatments and emotional struggles online, highlighting the need for professional support.

research Ruby laser-assisted hair removal: an ultrastructural evaluation of cutaneous damage

28 citations , December 1999 in “British Journal of Plastic Surgery”

research [An infant with short stature and red cheeks (Rothmund-Thomson syndrome)].

3 citations , December 1991 in “PubMed”

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets (HVDRR): Clinical Heterogeneity and Long-Term Efficacious Management of Eight Patients from Four Unrelated Arab Families with a Loss of Function VDR Mutation

research Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation

6 citations , June 2018 in “Journal of pediatric endocrinology & metabolism/Journal of pediatric endocrinology and metabolism”

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Bacillary Load and Reactional States in Leprosy: A Surge in Severity During the COVID Era?

research 070 Bacillary Load and Reactional States in Leprosy - A Surge in Severity the COVID Era?

October 2021 in “Journal of Investigative Dermatology”

The COVID-19 pandemic has led to more severe cases of Leprosy due to delayed medical care.

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