Treatment of Klippel-Feil syndrome with symptomatic atlantoaxial instability in a 7-year-old boy : A case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Treatment of Klippel-Feil syndrome with symptomatic atlantoaxial instability in a 7-year-old boy ; volume:53 ; number:10 ; day:8 ; month:8 ; year:2024 ; pages:799-804 ; date:10.2024
Die Orthopädie ; 53, Heft 10 (8.8.2024), 799-804, 10.2024
- Creator
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s00132-024-04537-z
- URN
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urn:nbn:de:101:1-2412122119183.487545928136
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:20 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Pepke, Wojciech
- Renkawitz, T.
- Hemmer, Stefan
- SpringerLink (Online service)
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“Clinical triad” findings in pediatric Klippel-Feil patients
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Mutation in MEOX1gene causes a recessive Klippel-Feil syndrome subtype
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome
Application of C2 subfacetal screws for the management of atlantoaxial dislocation in patients with Klippel-Feil syndrome characterized by a narrow C2 pedicle and high-riding vertebral artery
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Klippel-Feil-Syndrom
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Untersuchung zur Erblichkeit des Klippel-Feil'-Syndroms
Das sogenannte Klippel-Feil-Syndrom - Klinik, Pathogenese, Vererbung
“Clinical triad” findings in pediatric Klippel-Feil patients
Atlasassimilation kombiniert mit Klippel-Feil-Syndrom : Bericht e. Falles
Halswirbelkörper-Synostosen, Klippel-Feil-Syndrom: Wiederholungsrisiko für Kinder und Geschwister
Mutation in MEOX1gene causes a recessive Klippel-Feil syndrome subtype
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome
Application of C2 subfacetal screws for the management of atlantoaxial dislocation in patients with Klippel-Feil syndrome characterized by a narrow C2 pedicle and high-riding vertebral artery
Klippel–Feil Syndrome (KFS) with Multiple Cervical Anomalies Discovered Following Trauma
The Crossed Flexor Plantar Response in Patients with Klippel-Feil Syndrome
Klippel-Feil-Syndrom
Das Klippel-Feil-Syndrom
Untersuchung zur Erblichkeit des Klippel-Feil'-Syndroms
Das sogenannte Klippel-Feil-Syndrom - Klinik, Pathogenese, Vererbung
“Clinical triad” findings in pediatric Klippel-Feil patients
Atlasassimilation kombiniert mit Klippel-Feil-Syndrom : Bericht e. Falles
Halswirbelkörper-Synostosen, Klippel-Feil-Syndrom: Wiederholungsrisiko für Kinder und Geschwister
Mutation in MEOX1gene causes a recessive Klippel-Feil syndrome subtype
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome
Application of C2 subfacetal screws for the management of atlantoaxial dislocation in patients with Klippel-Feil syndrome characterized by a narrow C2 pedicle and high-riding vertebral artery
Klippel–Feil Syndrome (KFS) with Multiple Cervical Anomalies Discovered Following Trauma