Results 181 to 190 of about 219,473 (341)

Clinical Utility of a Droplet Digital PCR-Based Assay for Quantitative Detection of <i>Pneumocystis jirovecii</i> in Suspected Fungal Pneumonia. [PDF]

Infect Drug Resist
Jiang Z, Zhou Y, Huang H, Yuan Y, Tang Q, He C.   +5 more
europepmc   +1 more source

The involvement of PCP proteins in radial cell intercalations during Xenopus embryonic development.

Developmental Biology, 2015
O. Ossipova, C. Chu, Jonathan Fillatre, B. Brott, K. Itoh, S. Sokol   +5 more
semanticscholar   +1 more source

PCP [PDF]

, 2019
openaire   +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

Person-centered practice in the Portuguese healthcare system: A documentary study. [PDF]

PLoS One
Vareta D, Santana E, Oliveira C, Baixinho C, Ventura F.   +4 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

A sequential defense-nourishment strategy enabled by thermosensitive core-shell microneedles for synergistic tendon repair. [PDF]

Mater Today Bio
Fu M, Li J, Jiang Y, Shao Y, Wu D, Zhong S, Huang Z, Chen C, Guo J, Xie D, Zeng C.   +10 more
europepmc   +1 more source

Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profile and Associated Factors

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Evidence on developmental milestones in children with arthrogryposis multiplex congenita (AMC) under the age of five is scarce. This multisite cross‐sectional study described developmental status and examined factors associated with milestone attainment in 143 children aged 0–66 months from a pediatric AMC Registry.
Ahlam Zidan, Sophia C. Pasia, Emmanouil Rampakakis, Reggie Hamdy, Frank Rauch, Lauren C. Hyer, Joel Lerman, Haluk Altiok, Krister Freese, Cary Mielke, Sarah B. Nossov, Philip F. Giampietro, Thania Ordaz‐Robles, Noémi Dahan‐Oliel   +13 more
wiley   +1 more source

Pine Resin as a Natural Polymer Binder in Pine Cone-Reinforced Lightweight Concrete. [PDF]

Polymers (Basel)
Kistak C, Hassan AM, Bicer A, Celik N.
europepmc   +1 more source

PCP and Septins Compartmentalize Cortical Actomyosin to Direct Collective Cell Movement

Science, 2014
Asako Shindo, John B. Wallingford
semanticscholar   +1 more source