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Research 151–180 of 1000+
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Familial aggregation of phenotypic expression of premature hair hypopigmentation in the craniofacial region
- How safe and effective is minoxidil for familial baldness in women?
- Familial association of polycystic ovary syndrome (PCOS) in women attending the gynaecological endocrinology clinic at Groote Schuur Hospital
- Analysis of familial history in Chinese patients with androgenetic alopecia
- New familial association between ocular coloboma and loose anagen syndrome
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- 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
- Acne neonatorum and Familial Hyperandrogenism
- Cantú syndrome with coexisting familial pituitary adenoma
- A new familial presentation of dissecting cellulitis: The genetic implications on scarring alopecias
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- Vitiligo – Study In view of familial occurence
- BIOCHEMICAL FACTORS INFLUENCING FAMILIAL HIRSUTISM IN THE SOUTHERN REGION OF KPK
- Identification of Familial Infections Using Multilocus Microsatellite Typing in Tinea Corporis due to <i>Microsporum canis</i>
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Cutaneous xanthomas in homozygous familial hypercholesterolemia: A 12-year follow-up
- Delayed Diagnosis of Familial Adenomatous Polyposis-related Colon Cancer in an Adolescent with Coexisting Eating Disorder: A Case Report
- O cuidado à família de portadores de transtorno mental: visão dos trabalhadores
- Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)
- Precocious puberty: the unlikely herald of Familial adenomatous polyposis in a young girl
- Dominant dystrophic epidermolysis bullosa: Seven familial cases
- Effectiveness of Anastrozole and Cyproterone Acetate in Two Brothers with Familial Male Precocious Puberty
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- An alternative diagnostic method of eruptive vellus hair cysts: Report of a familial case with pruritus
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- A Mutation of the Androgen Receptor Associated with Partial Androgen Resistance, Familial Gynecomastia, and Fertility*