Results 31 to 40 of about 4,842,469 (101)

Achondroplasia Associated with Bilateral Keratoconus

open access: yes, 2012
We report a rare case of bilateral keratoconus in association with achondroplasia. A 26-year-old male, with a known case of achondroplasia, complained of bilateral gradual deterioration in vision for the past few years.
Ghada Y. Al Bin Ali   +3 more
core   +1 more source

Neuroimaging and calvarial findings in achondroplasia

open access: yes, 2020
Achondroplasia is the most common hereditary form of dwarfism and is characterized by short stature, macrocephaly and various skeletal abnormalities. The phenotypic changes are mainly related to the inhibition of endochondral bone growth.
Sarioglu, FATMA CEREN   +5 more
core   +1 more source

Labour market tax policy in the EMU [PDF]

open access: yes
Contents: 1. Forum Economique Franco-Allemand - Deutsch-Französisches Wirtschaftspolitisches Forum...1 -- 2. EMU and the Labour Market - A Speculative Assessment - Karl-Heinz Paqué...2 -- 3.
Deutsch-Französisches Wirtschaftspolitisches Forum (Ed.)
core  

Growth velocity and biological variables during puberty in achondroplasia

open access: yes, 2018
Background: Achondroplasia is the most common form of inherited disproportionate short stature. Cross-sectional design studies of height show that, during childhood, height standard deviation scores (SDS) declines steadily and reaches a
Paula Adamo   +2 more
core   +1 more source

Coronavirus: What next for Democracy? A report from the European Forum Alpbach

open access: yes, 2020
By Neus Vidal-Martí From 23 August to 3 September 2020, the 75th European Forum Alpbach was held as a 12-day online conference. The European Forum Alpbach is an interdisciplinary platform for science, politics, business and culture.
Forum Transregionale Studien
core  

Achondroplasia in the Premature Infant: An Elusive Diagnosis in the Neonatal Intensive Care Unit

open access: yes, 2017
Achondroplasia is a difficult prenatal diagnosis to make before the late second and third trimester. We describe two cases where an infant was born prematurely with no overt signs of achondroplasia. Despite multiple chest and abdominal radiographs during
Anna Blask   +3 more
core   +1 more source

The European legal forum : Forum iuris communis Europae.

open access: yes
Yr. 12 (2012) niet verschenen.Samensmelting van: The European legal forum. Section I, en: The European legal forum.

core  

Unilateral Frontosphenoidal Craniosynostosis with Achondroplasia: A Case Report

open access: yes, 2011
Isolated, premature fusion of the frontosphenoidal suture is rare. This report describes an unusual combination of frontosphenoidal craniosynostosis and achondroplasia.
Jerome L. Gorski   +2 more
core   +1 more source

Clinical, anthropometric, radiological and molecular characteristics of Egyptian achondroplasia patients [PDF]

open access: yes, 2009
Background: Achondroplasia is the most common form of non lethal skeletal dysplasia. It is a fully penetrant autosomal dominant disorder and the majority of cases are sporadic resulting from de novo mutations associated with advanced paternal age.
EL-Katoury, A IS   +6 more
core  

D4.5 Pan-European Policy Forum [PDF]

open access: yes, 2019
The one day Doing It Together Science (DITOs) Pan-European Forum took place on 3rd April 2019 at the Institut royal des Sciences Naturelles de Belgique (RBINS) in Brussels. The forum was attended by 113 representatives across the following sectors: civil
DITOs Consortium
core   +1 more source

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