A Giedion - Concepedia

Author

A Giedion

University Children's Hospital Zurich

Also Known As

A GIEDION, A Giedion, A. GIEDION, A. Giedion, Andres Giedion, J. I. Sebes, P. Beighton

Publications

Citations

H-Index

Concepts

All Affiliations

University Children's Hospital Zurich University of Zurich Johannes Gutenberg University Mainz Universitätskinderklinik

About

A Giedion is an author at University Children's Hospital Zurich specializing in medicine, orthopaedics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	25	1.5K
2	Anatomy	5	5	167
3	Education	1	1	33
4	Health Sciences	1	1	11
5	Natural Sciences	1	1	102

A Giedion

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
[Subacute and chronic "symmetrical" osteomyelitis]. A Giedion, W Holthusen, Masel Lf, PubMed Bone DiseaseRheumatologyOsteopathySurgical PathologyPathology	1972	417
Acute pulmonary X-ray changes in hyaline membrane disease treated with artificial ventilation and positive end-expiratory pressure (PEP) A Giedion, H. Haefliger, P. Dangel Pediatric Radiology Acute Lung InjuryHyaline Membrane DiseasePulmonary CirculationVentilationArtificial Ventilation	1973	173
Homozygous Mutations in IHH Cause Acrocapitofemoral Dysplasia, an Autosomal Recessive Disorder with Cone-Shaped Epiphyses in Hands and Hips Jan Hellemans, Paul Coucke, A Giedion, The American Journal of Human Genetics Cone-shaped EpiphysesHomozygous MutationsThumb HypoplasiaMendelian DisorderAutoimmune Disease	2003	147
A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs Albert Schinzel, A Giedion American Journal of Medical Genetics	1978	146
Autosomal-dominant transmission of the tricho-rhino-phalangeal syndrome. Report of 4 unrelated families, review of 60 cases. A Giedion, M Burdea, Z Fruchter, PubMed Tricho-rhino-phalangeal SyndromeAutosomal-dominant TransmissionUnrelated Families	1973	108
Spondyloepiphyseal dysplasia, corneal clouding, normal intelligence and acid β‐galactosidase deficiency John S. O’Brien, E Gugler, A Giedion, Clinical Genetics	1976	105
A glycine 375-to-cysteine substitution in the transmembrane domain of the fibroblast growth factor receptor-3 in a newborn with achondroplasia Andrea Superti‐Furga, B Steinmann, R Gitzelmann, European Journal of Pediatrics FibrosisDevelopmental BiologySignal TransductionMolecular PhysiologyGrowth Hormone	1995	102
The Pattern of Shortening of the Bones of the Hand in PHP and PPHP—A Comparison with Brachydactyly E, Turner Syndrome, and Acrodysostosis Andrew K. Poznanski, E A Werder, A Giedion, Radiology Thumb HypoplasiaBrachydactyly EPphp—a ComparisonOsteopathyMedicine	1977	93
Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweym�ller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome) Tero Pihlajamaa, Darwin J. Prockop, J�rg Faber, American Journal of Medical Genetics	1998	88
<i>RMRP</i> gene sequence analysis confirms a cartilage‐hair hypoplasia variant with only skeletal manifestations and reveals a high density of single‐nucleotide polymorphisms Luisa Bonafé, Katharina Schmitt, Georg Eich, Clinical Genetics	2002	87

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