Results 201 to 210 of about 346,758 (357)

Assessment of Autonomic Dysfunction in Patients With Empty Nose Syndrome Using the Composite Autonomic Symptom Scale-31. [PDF]

J Rhinol
Ryu SS, Kim DY, Jang YJ.
europepmc   +1 more source

A Core Head, Neck, and Neuroanatomy Syllabus for Physical Therapy Student Education

Clinical Anatomy, EarlyView.
ABSTRACT Head, neck, and neuroanatomy are essential components of physical therapy education due to their broad clinical applications. Detailed syllabi exist for medical students, yet none have been developed for physical therapy. This study aimed to produce an International Federation of Associations of Anatomists core head, neck, and neuroanatomy ...
Stephanie J. Woodley, Brooke Willoughby, Alexandra L. Webb, Natasha A. M. S. Flack, Laura Y. Whitburn   +4 more
wiley   +1 more source

Progress of diseases of the nose—B. A. Waddington Salem [PDF]

, 1903
M. D. Lederman
openalex   +1 more source

Heterozygous Med13l mice recapitulate a developmental growth delay and craniofacial anomalies seen in MED13L syndrome

Developmental Dynamics, EarlyView.
Abstract Background Gene transcription is crucial for embryo and postnatal development and is regulated by the Mediator complex. Mediator is comprised of four submodules, including the kinase submodule (CKM). The CKM consists of MED13, MED12, CDK8, and CCNC.
Anna K. Leinheiser, Timothy T. Nguyen, Kayla M. Henry, Mariela Rosales, Eric Van Otterloo, Chad E. Grueter   +5 more
wiley   +1 more source

Characterization of the different volatile organic compounds in human and ruminant milk using electronic nose analysis and headspace gas chromatography-mass spectrometry. [PDF]

Food Chem X
Zhu Z, Li D, Ahmad N, Chu T, Niu C, Zhang L, Song Y.   +6 more
europepmc   +1 more source

Pathogenesis and potential therapeutic targets of trichorhinophalangeal syndrome; lessons obtained from animal studies

Developmental Dynamics, EarlyView.
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki, Rinna Kanai, Sayuri Tatsuta, Shinichi Kawaguchi, Masatsune Itoh, Shinsuke Ohba, Makoto Abe   +6 more
wiley   +1 more source

Validity and Reliability of a French Version of the Empty Nose Syndrome 6-Item Questionnaire. [PDF]

J Clin Med
Maniaci A, Lechien JR.
europepmc   +1 more source

Hodgkin's Disease in the Nose

Hodgkin's Disease in the Nose
We report herein a very rare case of Hodgkin's disease which developed in the right nasal region and followed a peculiar clinical course. A 56 year old Japanese woman complained of right nasal obstruction and bleeding. The lesion first showed evidence of nasal polyp and progressed slowly, but became aggravated and advanced rapidly immediately before ...
openaire  

Interleukin (IL)‐5, Eosinophils and IL‐5 Pathway Inhibitors in Eosinophilic Granulomatosis with Polyangiitis.

Arthritis &Rheumatology, Accepted Article.
Alvise Berti, Christian Pagnoux
wiley   +1 more source

Synergistic Enhancement of Modified‐PVDF Humidity Sensitivity via Chemical Adsorption‐Ionic Conductivity and its Application in Intelligent Powered Air‐Purifying Respirator

ENERGY &ENVIRONMENTAL MATERIALS, EarlyView.
The study developed a PVDF/SiO2 humidity sensor with superhydrophobic properties and integrated the humidity sensor into the intelligent powered air‐purifying respirator (IPAPR) for breath monitoring. Coupled with the Gated Recurrent Unit (GRU) machine learning prediction algorithm, it enables feedforward control of the fan to achieve respiratory ...
Xinjian He, Hongwei Liu, Xianjie Xu, Xinkai Qi, Danhong Gao, Hanling Deng, Dusong Hou, Qianyao Lu, Lei Zhu, Sheng Huang   +9 more
wiley   +1 more source