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120-150 / 1000+ resultsresearch The efficacy of topical minoxidil 2% versus topical botanically derived inhibitors of 5 alpha reductase in treatment of female pattern hair loss by trichoscopy
research Genetic and molecular aspects of androgenetic alopecia
research Study of the international epidemiology of androgenetic alopecia in young caucasian men using photographs from the internet
![Baldness: Comprehensive aspects and its reassuring remedies](/images/research/88bb3368-74ce-4954-9ae1-4843d3b4485d/small/16491.jpg)
research Baldness: Comprehensive aspects and its reassuring remedies
There are effective treatments available for baldness.
![Polycystic ovary syndrome: etiology, pathogenesis and diagnosis](/images/research/e18ff8f5-c33d-4dd4-b723-d94737051586/small/14735.jpg)
research Polycystic ovary syndrome: etiology, pathogenesis and diagnosis
The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.
research Complex X chromosome rearrangement associated with multiorgan autoimmunity
A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.
![Omenn syndrome in a 10-month-old male with athymia and VACTERL association](/images/research/2d0af9c7-4493-467e-9ee8-1d69403fa0b8/small/32983.jpg)
research Omenn syndrome in a 10-month-old male with athymia and VACTERL association
A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.
![Dihydrotestosterone inhibits hair growth in mice by inhibiting insulin-like growth factor-I production in dermal papillae](/images/research/f68d4676-c2a3-4cdb-a792-ba65b03d7dba/small/26123.jpg)
research Dihydrotestosterone inhibits hair growth in mice by inhibiting insulin-like growth factor-I production in dermal papillae
Dihydrotestosterone (DHT) stops hair growth in mice by lowering a growth factor important for hair.
![The Rotterdam Study: 2012 objectives and design update](/images/research/95985cde-26c8-4051-ab39-3109710c53bb/small/16309.jpg)
research The Rotterdam Study: 2012 objectives and design update
The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.
![Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis](/images/research/e45f93eb-28ad-4743-bee2-3561e98ce94e/small/18874.jpg)
research Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.
![Integrative Analysis of Methylome and Transcriptome Reveals the Regulatory Mechanisms of Hair Follicle Morphogenesis in Cashmere Goat](/images/research/452b2c6a-5f11-4f9e-9540-6588c9542a7e/small/19292.jpg)
research Integrative Analysis of Methylome and Transcriptome Reveals the Regulatory Mechanisms of Hair Follicle Morphogenesis in Cashmere Goat
DNA methylation and long non-coding RNAs are key in controlling hair growth in Cashmere goats.
![An update on diagnosis and treatment of female pattern hair loss](/images/research/06f08f17-2638-4ccb-924d-1744523fe099/small/3339.jpg)
research An update on diagnosis and treatment of female pattern hair loss
Updated treatments for female hair loss include minoxidil, antiandrogens, hair transplants, and light therapy.
![Inherited Epidermolysis Bullosa: A Clinical Case](/images/research/f153d98e-e27b-4e8e-89e7-9bedd411590f/small/23951.jpg)
research Inherited Epidermolysis Bullosa: A Clinical Case
A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.
![Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer](/images/research/60413399-b02d-45fb-83df-da64533a29f7/small/19473.jpg)
research Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer
Stem cell plasticity is crucial for wound healing but can also contribute to cancer development.
![Clinical management of patients with<i>ASXL1</i>mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance](/images/research/1e39030d-d7c1-4a6b-bded-77c37327c101/small/34905.jpg)
research Clinical management of patients withASXL1mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance
Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.
![Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias](/images/research/9b07a087-1e2e-44fe-8615-e4bbd8a5a746/small/15996.jpg)
research Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.
![New Biomarkers to Evaluate Hyperandrogenemic Women and Hypogonadal Men](/images/research/46cd180b-5c14-4475-b27d-80adc67676b3/small/13683.jpg)
research New Biomarkers to Evaluate Hyperandrogenemic Women and Hypogonadal Men
The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.
![Noval advance of histone modification in inflammatory skin diseases and related treatment methods](/images/research/745c5b30-df56-4b1c-a9a0-6039ca9cf0ff/small/36102.jpg)
research Noval advance of histone modification in inflammatory skin diseases and related treatment methods
Histone modification is key in treating chronic inflammatory skin diseases.
![Efeitos do uso da finasterida sobre o volume prostático e dosagem sérica do PSA em pacientes jovens](/images/research/4fa77dde-9837-43f9-b100-495890c93a05/small/33126.jpg)
research Efeitos do uso da finasterida sobre o volume prostático e dosagem sérica do PSA em pacientes jovens
Finasteride reduces prostate size and PSA levels in young patients.
![Eating disorders](/images/research/5f810bcc-9891-4848-af81-ae929ec855ee/small/24250.jpg)
research Eating disorders
Eating disorders are serious, often undiagnosed conditions requiring early treatment, with anorexia being the most deadly and binge-eating the most treatable.
research A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.
![The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier](/images/research/af02ace6-9d19-4b67-8238-a6212ec298e5/small/20087.jpg)
research The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier
IL-1 family cytokines are crucial for skin defense and healing, but their imbalance can cause skin diseases.
![Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update](/images/research/b21eca90-5b5a-4ad6-9117-498d7d7128db/small/14594.jpg)
research Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.
![Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease](/images/research/c31384c1-cb33-4413-abd2-12050c1ff724/small/26144.jpg)
research Kin‐cohort analysis of LRRK2‐G2019S penetrance in Parkinson's disease
The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.
![Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)](/images/research/ee963c44-aab2-4039-88ec-c7f16ff84902/small/26149.jpg)
research Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)
The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.
![Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy](/images/research/568a76b2-8852-45ba-bbb3-c3fb87cc49a2/small/26158.jpg)
research Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.
![No evidence for <i>THAP1</i>/<i>DYT6</i> variants as disease modifiers in DYT1 dystonia](/images/research/2ee990ee-394f-4310-8440-6eae5d2958fe/small/26155.jpg)
research No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia
THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.
![Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia](/images/research/4c5849c1-4525-41b3-96b3-0a362902b4c0/small/26153.jpg)
research Mutation in 5′ upstream region of GCH I gene causes familial dopa-responsive dystonia
A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.
![A preliminary study of finasteride in Tourette syndrome](/images/research/c1e2332b-bb2a-4ec1-a25a-91758319e168/small/3082.jpg)
research A preliminary study of finasteride in Tourette syndrome
Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.