research Bureau of Legal Medicine and Legislation
Companies agreed to stop false advertising about their products' health benefits.
Search
for
Sort by
Research
750-780 / 1000+ results 
research Medico-Legal Corner
The document's conclusion cannot be summarized because the content is not accessible or understandable.
research Subject Index, Vol. 7,1994
research A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.
research 307 Dermatologic toxicities associated with chronic gamma-secretase inhibitor treatment for desmoid tumor
Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.
research N‑K SCIENCES IN 13 MONTHS: The Complete Bibliography — 335+ Publications Organized by Scientific Domain (February 2025 – March 2026)
research N‑K SCIENCES IN 13 MONTHS: The Complete Bibliography — 335+ Publications Organized by Scientific Domain (February 2025 – March 2026)
research Notes from the Editor Emeritus
The document could not be processed for a summary.
research Scalp dermoscopy of androgenetic alopecia in Asian people
research Hair growth-promoting effects of Stellera chamaejasme L. extract on C57BL/6 mice via induction of anagen phase genes
Stellera chamaejasme L. extract promotes hair growth by activating hair growth genes.
research A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
A gene mutation in mice causes severe skin disorder similar to a human condition.
research Preformulation studies of finasteride to design matrix systems for topical delivery
research The “Science of Aging, Part 2” Supplement
The document's conclusion cannot be provided because the document is not accessible or understandable.
research Contents Vol. 231, 2015
The document covers various dermatological treatments and conditions.
research A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.
research Salute to Surgeon of the Month
The document's conclusion cannot be provided because the content is not available.
research Salute to Surgeon of the Month
The document's conclusion cannot be provided because the content is not available.
research Dermatoscopy of hair shaft disorders
Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.
research TRPS1 mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.
research Meetings and Studies: British Association of Hair Restoration Surgeons 2011 business meeting
Unable to provide a summary as no conclusion is provided in the text.
research Table of Contents
research Table of Contents
research Table of Contents
research Table of Contents
research Table of Contents
research Table of Contents
research Table of Contents
research Table of Contents
research Table of Contents
