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Efficacy and Safety of Tracnil Administration in Patients with Dermatological Manifestations of PCOS: An Open-Label Single-Arm Study

research Efficacy and Safety of Tracnil™ Administration in Patients with Dermatological Manifestations of PCOS: An Open-Label Single-Arm Study

3 citations , March 2020 in “Dermatology Research and Practice”

Tracnil™, a mix of myo-inositol, folic acid, and vitamin D3, safely reduced acne, improved excessive hair growth, and fixed irregular periods in overweight women with PCOS.

research Trichotillomania/Hair Pulling Disorder

January 2015 in “The Encyclopedia of Clinical Psychology”

Habit reversal training effectively treats hair-pulling disorder in both adults and children.

research The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity

55 citations , November 2010 in “Journal of Allergy and Clinical Immunology”

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

research Severe, Disfiguring, Pityriasis Rubra Pilaris in a Woman in the Dominican Republic

10 citations , October 2015 in “Journal of the International Association of Providers of AIDS Care”

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

research Focal Asymptomatic Hair Loss in an Adolescent: A Case Report

December 2019 in “Journal of pediatrics & neonatology”

A 13-year-old boy had a rare, stable type of hair loss with little chance of regrowth, but treatment is available for looks.

Detection of a Novel Missense Mutation in Atrichia with Papular Lesions

research Detection of a Novel Missense Mutations in Atrichia with Papular Lesions

4 citations , January 2011 in “Annals of Dermatology”

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

research Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament

27 citations , November 2007 in “Genomics”

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

research 6601 A Case of Recurrent Painless Thyroiditis and Discussion of Management

October 2024 in “Journal of the Endocrine Society”

Managing recurrent painless thyroiditis is challenging and should be personalized based on episode frequency, severity, symptoms, and patient preferences.

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 VDRi> 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.

research Type II Keratins Are Phosphorylated on a Unique Motif during Stress and Mitosis in Tissues and Cultured Cells
80 citations , June 2002 in “Molecular Biology of the Cell”

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

research Dormant tumor cells in ret transgenic mouse melanoma model and their interaction with memory T cells
January 2012 in “heiDOK (Heidelberg University)”

Dormant melanoma cells in mice interact minimally with memory T cells due to a suppressive tumor environment.

research Treatment of insulin resistance with tirzepatide leading to improvement of hair loss
12 citations , June 2024 in “JAAD Case Reports”

Tirzepatide may improve hair loss by reducing insulin resistance.

research Dermoscopic Findings and Their Therapeutic Implications in Trichostasis Spinulosa: A Retrospective Study of 306 Patients
13 citations , January 2018 in “Skin Appendage Disorders”

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

research Diffuse hypotrichosis from early childhood
September 2016 in “Journal of The American Academy of Dermatology”

The girl has a genetic hair condition causing thin hair since childhood.

research Combining 308-monochromatic excimer phototherapy with monthly IM triamcinolone acetonide for the treatment of resistant alopecia totalis
2 citations , December 2020 in “American Journal of Dermatological Research and Reviews”

The combination therapy was effective and well-tolerated, especially in young patients.

research Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
11 citations , March 2021 in “The journal of investigative dermatology/Journal of investigative dermatology”

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

research Possible Involvement of Skin‐Resident Memory T Cells in Refractory Chronic Alopecia Areata
January 2026 in “Experimental Dermatology”

Skin-resident memory T cells may contribute to chronic alopecia areata and baricitinib could be a potential treatment.

research TRICHOSTASIS SPINULOSA
14 citations , May 1979 in “International Journal of Dermatology”

Trichostasis spinulosa mainly affects the nose, with many tiny hairs in one follicle, possibly influenced by hormones and sunlight.

research Pathogenesis and management of TRPV3-related Olmsted syndrome
December 2024 in “Frontiers in Genetics”

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

research PRP versus intralesional triamcinolone for alopecia areata comparative study
January 2024 in “International Journal of Dermatology Research”

PRP is more effective than triamcinolone for treating alopecia areata.

research Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
February 2024 in “bioRxiv (Cold Spring Harbor Laboratory)”

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

research Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
44 citations , February 2012 in “The journal of neuroscience/The Journal of neuroscience”

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

research Clinical and Trichoscopic Characteristics in a Case of Congenital Triangular Alopecia
December 2020

Trichoscopic examination is crucial for diagnosing congenital triangular alopecia.

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 Successful Treatment of Temporal Triangular Alopecia by Hair Restoration Surgery Using Follicular Unit Transplantation
16 citations , June 2009 in “Dermatologic Surgery”

A 17-year-old boy with Temporal Triangular Alopecia successfully grew new hair after a hair restoration surgery using follicular unit transplantation.

research ROBERTSONIAN TRANSLOCATION PATIENT WITH RECURRENT MISCARRIAGE
June 2020 in “Zenodo (CERN European Organization for Nuclear Research)”

Robertsonian translocation can cause recurrent miscarriages.

research Homozygous missense mutation in theLIPHi>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
2 citations , December 2013 in “Journal of dermatology”

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

research Alopecia totalis successfully treated with modified platelet-rich plasma therapy in a patient recalcitrant to traditional treatment modalities
2 citations , January 2021 in “Clinical dermatology review”

Modified PRP therapy successfully treated severe alopecia unresponsive to traditional methods.

research In situ detection of retinoid-X receptor expression in normal and psoriatic human skin
42 citations , August 1995 in “British journal of dermatology/British journal of dermatology, Supplement”

RXR-alpha is strongly expressed in both normal and psoriatic skin and may help in skin cell differentiation and hair growth.

research The association of Wnt – Factor TCF7L2 (TCF4) gene polymorphism and treated Alopecia Areata (Platelet rich plasma Vs conventional)
February 2024 in “Zagazig University Medical Journal”

TCF7L2 gene polymorphism is linked to alopecia areata, but it doesn't affect the success of PRP or conventional treatments.

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