research A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.
Search
for
Sort by
Research
150-180 / 1000+ results research 710 BIOMARKERS OF SUNITNIB CLINICAL RESPONSE IN METASTATIC RENAL CLEAR CELL CARCINOMA PATIENTS
research Androgenetic Alopecia-Reply
Unable to summarize document.
research Cyberspace Chat: Scalp biopsies: to refer or not to refer?
The conclusion cannot be provided because the document is not accessible.
research Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
Specific gene variants affect wool traits in Chinese Tan sheep.
research SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.
research A Look at the 6th Annual Live-Surgery Workshop
The document's conclusion cannot be provided because the document is not accessible or understandable.
research Scalp dermoscopy of androgenetic alopecia in Asian people
research Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.
research Arbete i arbetslag och arbetsenheter inom grundskolan
Topical 0.1% tacrolimus improved a rare ear condition in cats.
research Gestational safety: No time for a pregnant pause
The document's conclusion cannot be provided because the document is not available to parse.
research 499 Possible involvement of skin resident memory T cells in refractory alopecia areata
research 탈모 치료에 관한 최신 동향
I'm sorry, but I can't process documents in Korean. If you provide an English text, I'd be happy to summarize the conclusion for you.
research Finasteride
research President's Message
The document's content could not be processed.
research President's Message
The document's content could not be processed.
research President's Message
The document's content could not be processed.
research androgenetic alopecia, n.
The document's conclusion cannot be determined from the provided text.
research Polymorphisms and association of FAT1 gene with wool quality traits in Chinese Merino sheep
The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.
research Doctor’s (patient’s) guide to estimating transplant grafts
The document could not be processed to provide a conclusion.
research The Efficacy and Safety of AP-FHG0604T on Female Pattern Hair Loss: A Randomized Double-blind Placebo-controlled Clinical Trial
research 42736 Safety Assessments in the Multinational Phase 3 THRIVE-AA1 Trial with CTP-543 (Deuruxolitinib) in Adult Patients with Moderate to Severe Alopecia Areata
The THRIVE-AA1 trial assessed the safety of CTP-543, a JAK1/JAK2 inhibitor, in 706 adult patients with moderate to severe alopecia areata. Participants were randomized to receive either a placebo, 8 mg BID, or 12 mg BID of CTP-543 for 24 weeks. Common adverse events included headache, nasopharyngitis, and upper respiratory tract infections. Serious adverse events were rare, with only one possibly related to CTP-543. The incidence and severity of adverse events were similar across the treatment groups, and no significant trends were observed in vital signs or ECG results. The study concluded that both doses of CTP-543 were generally well tolerated, with an encouraging safety profile for treating alopecia areata.
research First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.
research Surgical Assistants Editor’s Message
The document's conclusion cannot be provided because the content is not accessible.
research Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.
research To megasession or not to megasession: That seems to be the question
The document's conclusion cannot be provided because the content is not available.
research Meeting Announcement
research Temporal Triangular Alopecia: Report of Five Cases in Asian Children
Temporal triangular alopecia is a non-scarring hair loss seen in some Asian children.
research AB089. What should we know role of finasteride in erectile dysfunction?
research Megatransplants in Transition: A Pictorial Review
The document's conclusion cannot be provided because the content is not available to parse.