Results 301 to 310 of about 450,295 (383)

Trajectory and asymmetry of lower limb joint moments during normal and blindfolded gait. [PDF]

J Phys Ther Sci
Komuro N, Hirosawa A, Sano T, Mohara A, Nakamura T, Fukunaga M, Homma Y, Kakizaki F.   +7 more
europepmc   +1 more source

Atlas of the dragonflies of Britain and Ireland [PDF]

, 1996
Eversham, B. C., Merritt, R., Moore, N. W.   +2 more
core  

Examples of thorax segmentation results for COVID-19 and other viral pneumonia CXRs on th hold test set, with columns displaying the original chest X-ray, ground truth mask, predicted thorax mask, and the overlay of the predicted mask on the original image.

Nastaran Enshaei (9405653), Arash Mohammadi (9405641), Farnoosh Naderkhani (9405647), Nick Daneman (138878), Rawan Abu Mughli (21807644), Reut Anconina (21807647), Ferco H. Berger (21807650), Robert Andrew Kozak (21807653), Samira Mubareka (80688), Ana Maria Villanueva Campos (21807656), Keshav Narang (21807659), Thayalasuthan Vivekanandan (21807662), Adrienne Kit Chan (21807665), Philip Lam (20210669), Nisha Andany (11056596), Anastasia Oikonomou (9405635)   +15 more
openalex   +1 more source

Clinical Presentation of the Longest Reported Living Individual With Bent Bone Dysplasia—FGFR2‐Related

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates, Pardeep Gill, Matthew Choi, Frances Mahon, Blake Yarascavitch, Audrey Lim, Resham Ejaz   +6 more
wiley   +1 more source

Exertion-Induced Spontaneous Pneumomediastinum in a Healthy Young Male: A Case Report. [PDF]

Cureus
Zahid MT, Afzal S.
europepmc   +1 more source

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source

Development of a real-time multi-scenario monitoring method for respiratory motion based on capacitive sensors. [PDF]

Precis Radiat Oncol
Wang Y, Li B, Xiao X, Lou Z, Liu K, Ge H.   +5 more
europepmc   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

7T ¹⁹F/¹H MRI with perfluorocarbon-labeled immune cells in pigs: Pilot results with a dedicated twin-array system with pTX support. [PDF]

Magn Reson Med
Terekhov M, Elabyad IA, Hamid MA, Jabbarigargari F, Grampp R, Keshtkar M, Stadtmüller A, Ulm G, Dembski S, Frey A, Hofmann U, Bauer WR, Schreiber LM.   +12 more
europepmc   +1 more source