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Ralf Oheim (1977-)

Orthopäde

Name	Ralf Oheim
Time	1977- (Date of birth and death)
Place	Rostock (Geburtsort) Deutschland
Gender	männlich
Academic degree	Dr. med. (Univ. Rostock) (2006)
Profession	Orthopäde (characteristic profession) Arzt
Variant	R. Oheim
Related	Universitätsklinikum Hamburg-Eppendorf Osteologie (Thema)
Further information	Univ. Hamburg, Medizinische Fak., Universitätsklinikum Hamburg-Eppendorf, Zentrum für Experimentelle Medizin, Oberarzt am Inst. für Osteologie und Biomechanik Habil. Fach Orthopädie & Unfallchirurgie an der Univ. Lübeck
Record type	Person
GND-Identifier	133493210
Record ID	133493210
Involved in show all Relevant genetic variants are common in women with pregnancy and lactation-associated osteoporosis (PLO) and predispose to more severe clinical manifestations Comparison of Motion Grading in 1,000 Patients by First- and Second-Generation HR-pQCT: A Propensity Score Matched Cohort Study Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI) Beneficial effects of denosumab on muscle performance in patients with low BMD: a retrospective, propensity score-matched study Clinical and Radiological Characterization of Patients with Immobilizing and Progressive Stress Fractures in Methotrexate Osteopathy Bilateral Looser zones or pseudofractures in the anteromedial tibia as a component of medial tibial stress syndrome in athletes Whole-Exome Sequencing Identifies Novel Compound Heterozygous ZNF469 Mutations in Two Siblings with Mild Brittle Cornea Syndrome Humangenetische Zeitenwende in der Osteologie Impaired Bone Microarchitecture in Patients with Hereditary Hemochromatosis and Skeletal Complications Genetische Ursachen und Therapie der Osteogenesis imperfecta Die aktuelle Versorgungssituation von Patientinnen und Patienten mit seltenen Knochenerkrankungen an Universitätskliniken in Deutschland Von der Initiative (der Deutschen Gesellschaft für Osteologie [DGO]) zum Netzwerk: Vorstellung des deutschsprachigen Netzwerks für Seltene Osteopathien (NetsOs) Monogene frühmanifeste Osteoporose und Altersosteoporose – ein Kontinuum Bone microstructure is significantly altered in CRPS-affected distal tibiae as detected by HR-pQCT: a retrospective cross-sectional study Low physical performance determined by chair rising test muscle mechanography is associated with prevalent fragility fractures Comparison of Bone Microarchitecture Between Adult Osteogenesis Imperfecta and Early-Onset Osteoporosis Clinical Significance of DXA and HR-pQCT in Autosomal Dominant Osteopetrosis (ADO II) Is centrally induced alveolar bone loss in a large animal model preventable by peripheral hormone substitution? Deterioration of teeth and alveolar bone loss due to chronic environmental high-level fluoride and low calcium exposure Surgical therapy of extensive knee joint empyema: mid-term results after two-stage versus one-stage procedures Großtiermodelle humaner Knochenmasseverlustsyndrome : Bestandsaufnahme，Weiterentwicklung und skelettale Charakterisierung klinikrelevanter Schafmodelle Arthroscopic-assisted removal of proximal tibia locking plates Homologe Rekombination des NPC1-Gens in humanen Zellen : ein Modell für die Analyse zellulärer Konsequenzen verschiedener Mutationen

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Ralf Oheim (1977-)

Relevant genetic variants are common in women with pregnancy and lactation-associated osteoporosis (PLO) and predispose to more severe clinical manifestations

Comparison of Motion Grading in 1,000 Patients by First- and Second-Generation HR-pQCT: A Propensity Score Matched Cohort Study

Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI)

Beneficial effects of denosumab on muscle performance in patients with low BMD: a retrospective, propensity score-matched study

Clinical and Radiological Characterization of Patients with Immobilizing and Progressive Stress Fractures in Methotrexate Osteopathy

Bilateral Looser zones or pseudofractures in the anteromedial tibia as a component of medial tibial stress syndrome in athletes

Whole-Exome Sequencing Identifies Novel Compound Heterozygous ZNF469 Mutations in Two Siblings with Mild Brittle Cornea Syndrome

Humangenetische Zeitenwende in der Osteologie

Impaired Bone Microarchitecture in Patients with Hereditary Hemochromatosis and Skeletal Complications

Genetische Ursachen und Therapie der Osteogenesis imperfecta

Die aktuelle Versorgungssituation von Patientinnen und Patienten mit seltenen Knochenerkrankungen an Universitätskliniken in Deutschland

Von der Initiative (der Deutschen Gesellschaft für Osteologie [DGO]) zum Netzwerk: Vorstellung des deutschsprachigen Netzwerks für Seltene Osteopathien (NetsOs)

Monogene frühmanifeste Osteoporose und Altersosteoporose – ein Kontinuum

Bone microstructure is significantly altered in CRPS-affected distal tibiae as detected by HR-pQCT: a retrospective cross-sectional study

Low physical performance determined by chair rising test muscle mechanography is associated with prevalent fragility fractures

Comparison of Bone Microarchitecture Between Adult Osteogenesis Imperfecta and Early-Onset Osteoporosis

Clinical Significance of DXA and HR-pQCT in Autosomal Dominant Osteopetrosis (ADO II)

Is centrally induced alveolar bone loss in a large animal model preventable by peripheral hormone substitution?

Deterioration of teeth and alveolar bone loss due to chronic environmental high-level fluoride and low calcium exposure

Surgical therapy of extensive knee joint empyema: mid-term results after two-stage versus one-stage procedures

Großtiermodelle humaner Knochenmasseverlustsyndrome : Bestandsaufnahme，Weiterentwicklung und skelettale Charakterisierung klinikrelevanter Schafmodelle

Arthroscopic-assisted removal of proximal tibia locking plates

Homologe Rekombination des NPC1-Gens in humanen Zellen : ein Modell für die Analyse zellulärer Konsequenzen verschiedener Mutationen