Search
for
Sort by
Research 601–630 of 1000+
- Differences in Demographic and Clinical Characteristics Among Subtypes of Female Pattern Hair Loss
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- The clinical spectrum of parathyroid disease
- Type II Vitamin D Dependent Rickets: A Case Report
- Paraneoplastic alopecia associated with internal malignancies in the cat
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Multidimensional assessment of adverse events of finasteride：a real-world pharmacovigilance analysis based on FDA Adverse Event Reporting System (FAERS) from 2004 to April 2024
- Central hair loss in African American women: Incidence and potential risk factors
- Self-Amplifying RNA Approach for Protein Replacement Therapy
- Myeloma, Paraproteinemias, and the Skin
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Diseases of Periocular Hair
- Molecular pathology of skin adnexal tumours
- Cytostatics and immunosuppressive drugs
- Female Androgenetic (?) Alopecia
- Peter Kynaston Thomas, 28 June 1926–25 January 2008
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- [ADRENOCORTICAL CARCINOMA].
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- WNT Signaling in Disease
- Role of ACE2 polymorphism in COVID-19: impact of age
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Hair shaft disorders in children – An update