Results 181 to 190 of about 48,690 (312)

Short foot exercises for flatfoot therapy: Status and prospects. [PDF]

Sci Prog
Yang H, Liu C, Yao K, Yang J, Wang Y, Sun C, Li P, Dong H.   +7 more
europepmc   +1 more source

Maternal smoking and deformities of the foot: results of the EUROCAT Study. European Registries of Congenital Anomalies.

American Journal of Public Health, 1998
J. Reefhuis, H.E.K. de Walle, M. C. Cornel   +2 more
semanticscholar   +1 more source

Prevalence and Patterns of Permanent Tooth Agenesis in Patients With Crouzon or Apert Syndrome: A Systematic Review and Meta‐Analysis

Orthodontics &Craniofacial Research, Volume 29, Issue 1, Page 1-11, February 2026.
ABSTRACT Crouzon and Apert syndromes are rare syndromic craniosynostoses frequently associated with craniofacial and dental anomalies, including tooth agenesis. Although individual studies have reported tooth agenesis prevalence data in specific populations, no attempts have been made to systematically synthesise these data.
M. Cecilia Becerril Santos, Edwin M. Ongkosuwito, Alexandra K. Papadopoulou, Gregory S. Antonarakis   +3 more
wiley   +1 more source

Multilevel Laminectomy for Lumbar Spinal Stenosis With Low Back Pain in Achondroplasia: A Case Report. [PDF]

Am J Case Rep
Kapetanakis S, Chatzivasiliadis M, Koukos C, Tsioulas P, Siopis C, Gkantsinikoudis N.   +5 more
europepmc   +1 more source

Impact of the Ilizarov apparatus on external fixation: Current modifications of the 75-year-old orthopedic tool. [PDF]

World J Orthop
Sutyagin I, Malkova TA.
europepmc   +1 more source

Grice Arthrodesis and Arthroereisis in the Surgical Management of Pediatric Flatfoot: Radiological Outcomes and Limitations. [PDF]

J Clin Med
Marie H, Herdea A, Marica RI, Ulici A.
europepmc   +1 more source

Kinematic characterization of residual deformities in idiopathic clubfoot initially treated with the Ponseti method: Gait analysis using the Heidelberg Foot Model. [PDF]

J Child Orthop
Chen Q, Salami F, Putz C, Wolf SI.
europepmc   +1 more source

Classification and developmental biology of congenital anomalies of the hand and upper extremity [PDF]

, 2009
Manske, Paul R., Oberg, Kerby C.
core   +2 more sources

Malformation Pattern and Molecular Findings in the <i>FGFR1</i>-Related Hartsfield Syndrome Phenotype. [PDF]

Med Sci (Basel)
Gaudioso F, Pascolini G.
europepmc   +1 more source

A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis [PDF]

, 2017
et al,, Grange, Dorothy K
core   +2 more sources