Results 81 to 90 of about 11,048 (255)

Wildervanck syndrome [PDF]

open access: yes, 2008
O artigo relata o caso clínico de uma criança do sexo feminino, cinco anos de idade que apresenta a rara síndrome de Wilderwanck que consiste da síndrome de Klippel-Feil associada à síndrome de Duane e deficiência auditiva.
CAPELLA, João Luís Curvacho   +2 more
core   +2 more sources

Humeroradial Synostosis: An Updated Classification and Differential Diagnosis Based on Genetic Aetiology

open access: yesClinical Genetics, Volume 108, Issue 4, Page 379-392, October 2025.
The proposed updated classification of humeroradial synostosis is based on the molecular pathways of the genes involved: (1) chondrogenesis and osteogenesis; (2) limb development and patterning; (3) genome regulation. Thus, pathologies belonging to the same molecular type may have overlapping clinical phenotypes, helping to structure the diagnostic ...
Fiona Leduc   +5 more
wiley   +1 more source

A Scoping Review of Human Teratogens and Their Impact on the Developing Brain: A Contribution From the ConcePTION Project

open access: yesBirth Defects Research, Volume 117, Issue 9, September 2025.
ABSTRACT Certain medications, when used during pregnancy, are known to impact human prenatal development. Historically, little attention has been given to the impact of in utero exposure on the developing brain, despite the significance of known teratogen‐induced neurodevelopmental difficulties.
M. Bluett‐Duncan   +14 more
wiley   +1 more source

Psychosocial and quality of life outcomes of prosthetic auricular rehabilitation with CAD/CAM technology. [PDF]

open access: yes, 2014
published_or_final_versio
Cheung, LK   +5 more
core   +1 more source

Neonatal Epidermolytic Ichthyosis Caused by a KRT10 Mutation (c.467G>A, p.Arg156His): A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT We present a neonatal case of skin blisters and erythema. While epidermolysis bullosa was initially suspected, immunofluorescence antigen mapping and genetic testing confirmed epidermolytic ichthyosis, with a heterozygous pathogenic variant in the KRT10 gene (c.467G>A, p.Arg156His).
Elke Smits   +4 more
wiley   +1 more source

International Consensus Recommendations on Microtia, Aural Atresia and Functional Ear Reconstruction.

open access: yesThe journal of international advanced otology, 2019
The aim of this report is to provide international recommendations for functional ear reconstruction in patients with microtia and aural atresia.
Tian-Yu Zhang   +8 more
semanticscholar   +1 more source

Radiological Society of North America (RSNA) 3D printing Special Interest Group (SIG): Guidelines for medical 3D printing and appropriateness for clinical scenarios [PDF]

open access: yes, 2014
Este número da revista Cadernos de Estudos Sociais estava em organização quando fomos colhidos pela morte do sociólogo Ernesto Laclau. Seu falecimento em 13 de abril de 2014 surpreendeu a todos, e particularmente ao editor Joanildo Burity, que foi seu ...
Burity, Joanildo   +2 more
core   +2 more sources

Fibrinvernetzte Knorpel- und Kunststoffspäne zur Ohrmuschelrekonstruktion [PDF]

open access: yes, 1981
Bei der Ohrmuschelrekonstruktion werden vom Transplantat hohe Formbeständigkeit und gute Verträglichkeit verlangt. Es wurde untersucht, ob diese Forderungen von einem Gemisch aus geraspeltem, konserviertem Knorpel und gerinnungsaktivem Plasmaprotein ...
Berghaus, Alexander, Handrock, M.
core  

MICROTIA IN A LARGE WHITE YORKSHIRE PIGLET- A CASE REPORT

open access: diamond, 2021
M. Arul Prakash   +4 more
openalex   +1 more source

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