Results 141 to 150 of about 233,196 (250)

Sex-Discordant Monochorionic Dizygotic Twins After Double Blastocyst Transfer: Blood Chimerism Demonstrated by Multimodal Genetic Testing. [PDF]

J Obstet Gynaecol Res
Yuki K, Taura Y, Morishita H, Sugiura T, Kido S, Nakashima Y, Tocan V, Inoue Y, Kato K.   +8 more
europepmc   +1 more source

Epidemiological survey on frequency of involvement of atypical pathogens in respiratory infections in outpatients

, 2006
呼吸器感染症の初診時における，非定型病原体（Chlamydophila pneumoniae，Chlamydophila psittaci，Mycoplasma pneumoniae，Legionella pneumophila）の関与率を血清抗体価および尿中抗原検出により検討した。　2003年4月から6月に全国4地域（長崎，岡山，新潟，仙台）の開業医院59施設を呼吸器感染症（肺炎，気管支炎，咽頭・喉頭炎，扁桃炎）で受診した20歳以上の初診外来患者532症例を解析対象とした ...
平潟, 洋一, 渡辺, 彰, 二木, 芳人, 青木, 信樹, 河野, 茂   +4 more
core  

Small lesion, big challenge? Diagnosis of small diameter melanocytic lesions by dermatologists using AI support

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background Dermoscopy enhances melanoma detection, but small‐diameter melanomas (SDMs) remain diagnostically challenging. Convolutional neural networks (CNNs) may detect subtle patterns beyond human perception. This study evaluates how lesion diameter influences the diagnostic accuracy of dermatologists, with and without CNN support.
Anastasia Sophie Vollmer, Gianluca Nazzaro, Julia Katharina Winkler, Giuseppe Argenziano, Aimilios Lallas, Katharina Susanne Kommoss, Andreas Blum, Wilhelm Stolz, Carlo Maronese, Serena Giacalone, Cristina B Spigariolo, Gabriele Roccuzzo, Gianluca Avallone, Stefania Guida, Gabriella Brancaccio, Paolo Broganelli, Giovanni Pellacani, Francesca Farnetani, Emanuela Passoni, Angelo V Marzano, Alexander Enk, Holger Andreas Haenssle   +21 more
wiley   +1 more source

Androgen insensitivity syndrome: A case report. [PDF]

Medicine (Baltimore)
Zhang Y, Wang H, Xiao Z.
europepmc   +1 more source

Concurrent validity and agreement of Bayley‐4, AIMS, and HINE assessments in 1‐year‐old children

Developmental Medicine &Child Neurology, EarlyView.
In this cross‐sectional study of children around 1‐year‐old, the Bayley‐4 showed concurrent validity and moderate to substantial agreement with the AIMS and the HINE in both clinical and home settings. Abstract Aim To examine concurrent validity between the Bayley Scales of Infant and Toddler Development, Fourth Edition (Bayley‐4) gross motor subtest ...
Weiyang Deng, Bahda Hoang, Meaghan Rubsam, Gabriela Lopez, Megan K. O'Brien, Theresa Sukal‐Moulton, Barbara Sargent, Colleen Peyton, Elizabeth Hoffman, Samuel Carey, Nicole Pouppirt, Raye‐Ann de Regnier, John A. Rogers, Richard L. Lieber, Arun Jayaraman   +14 more
wiley   +1 more source

A Case of Pemphigus Herpetiformis in a 10-Year-Old Child. [PDF]

Clin Cosmet Investig Dermatol
Hao Z, Fan L, Song H, Xiang Z.
europepmc   +1 more source

Transpupillary thermotherapy for atypical central serous chorioretinopathy

, 2012
Ryosuke Kawamura1,2, Hidenao Ideta1, Hideyuki Hori1, Kenya Yuki2, Tsuyoshi Uno1, Tatsurou Tanabe1, Kazuo Tsubota2, Tsutomu Kawasaki11Ideta Eye Hospital, Kumamoto, Japan; 2Keio University, School of Medicine, Department of Ophthalmology, Tokyo ...
Kawasaki T, Yuki K, Hori H, Kawamura R, Tsubota K, Uno T, Tanabe T, Ideta H   +7 more
core  

Neuropathic pain in cerebral palsy and related genetic conditions: A scoping review of prevalence, characteristics, and management

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aim To map existing evidence on neuropathic pain in cerebral palsy (CP) and related genetic conditions, including prevalence, descriptors, assessment methods, and management. Method Following prospective registration, five databases (Ovid MEDLINE, Embase, CINAHL, Web of Science, Google Scholar) were searched in June 2025.
Aayushi Khillan, Sanya Verma, Hannah Yeomans, Karen Bau, Caitlin Doyle, Monica S. Cooper, David J. Amor, Carolyn Berryman, Adrienne Harvey   +8 more
wiley   +1 more source

Spectrum and clinical profile of disorders of sex development: A 10 year experience at a tertiary care center. [PDF]

Pak J Med Sci
Aslam N, Aftab S, Naseer Khan B, Noor-E-Hira.   +3 more
europepmc   +1 more source

Multisystem developmental abnormalities and insulin resistance in ADTKD‐HNF1B with the p.E105K variant: A clinical conundrum

Diabetic Medicine, EarlyView.
Abstract Aims HNF1B variants cause autosomal dominant tubulointerstitial kidney disease (ADTKD‐HNF1B), but the phenotypic spectrum of variants of uncertain significance (VUS) remains incompletely defined. We aimed to characterise the multisystem phenotype associated with the HNF1B p.E105K variant and to examine the mechanism underlying insulin ...
YunZe Wang, KangChun Xu, PengFei Liu, Bin Wang, Yan Yang, ShanZhai Wei   +5 more
wiley   +1 more source