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Lothar Seefried (1976-)

Orthopäde

Name	Lothar Seefried
Time	1976- (Date of birth and death)
Place	Würzburg (Wirkungsort) Deutschland
Gender	männlich
Academic degree	Dr. med. habil.
Profession	Orthopäde (characteristic profession)
Related	Orthopädische Klinik König-Ludwig-Haus
Further information	Habilitation Fach Orthopädie und Unfallchirurgie an der Medizinischen Fakultät der Univ. Würzburg (2022); Facharzt für Orthopädie und Unfallchirurgie, Osteologe (DVO), Leiter Schwerpunkt Osteologie/Osteoporose im König-Ludwig-Haus Würzburg
Source	Die Hypophosphatasie im Erwachsenenalter - 2022 Klinik-website: https://www.koenig-ludwig-haus.de/medizin-und-pflege/orthopaedische-schwerpunkte/osteologie--osteoporose/team/index.html (Stand: 13.03.2024)
Record type	Person
GND-Identifier	124903908
Record ID	124903908
Involved in show all XLH Matters 2024: expert insights and practical tools for enhancing care of people living with X-linked hypophosphataemia Developing a Standardised Dataset for Natural History Studies in Fibrous Dysplasia/McCune-Albright Syndrome Grading Pseudofractures—The “Breach–Beak–Bump–Bridge” Approach Diagnosis and Treatment of Hypophosphatasia Publisher Correction: Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia Anticipated effects of burosumab treatment on long-term clinical sequelae in XLH: expert perspectives Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults Impact of muscular symptoms and/or pain on disease characteristics, disability, and quality of life in adult patients with hypophosphatasia: A cross-sectional analysis from the Global HPP Registry Whole genome sequencing in adults with clinical hallmarks of hypophosphatasia negative for ALPL variants Correction: Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults Effectiveness of asfotase alfa for treatment of adults with hypophosphatasia: results from a global registry Clinical Profiles of Children with Hypophosphatasia prior to Treatment with Enzyme Replacement Therapy: An Observational Analysis from the Global HPP Registry Challenges in the management of tumor-induced osteomalacia (TIO) Relevant genetic variants are common in women with pregnancy and lactation-associated osteoporosis (PLO) and predispose to more severe clinical manifestations Proposed diagnostic criteria for the diagnosis of hypophosphatasia in children and adolescents: results from the HPP International Working Group The challenge of hypophosphatasia diagnosis in adults: results from the HPP International Working Group Literature Surveillance Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH) Efficacy of Zoledronic Acid in the Treatment of Nonmalignant Painful Bone Marrow Lesions: A Triple‐Blind, Randomized, Placebo‐Controlled Phase III Clinical Trial (ZoMARS) Einfluss von Vibrationstraining auf körperliche Leistungsfähigkeit, Alltagsaktivität und Lebensqualität von Patienten mit monoklonaler Gammopathie Supplement: Impaired Physical Performance in X-linked Hypophosphatemia is not caused by depleted muscular phosphate stores Clinical profiles of treated and untreated adults with hypophosphatasia in the Global HPP Registry Lower limb bone geometry in adult individuals with X-linked hypophosphatemia: an observational study Feasibility of simple exercise interventions for men with osteoporosis – A prospective randomized controlled pilot study Insuffizienzfraktur der Klavikula nach Implantation einer inversen Schulterendoprothese Sarcopenia and Malnutrition Screening in Female Osteoporosis Patients — A Cross-Sectional Study X-chromosomale Hypophosphatämie - Phosphatdiabetes - XLH X-chromosomale Hypophosphatämie - Phosphatdiabetes - XLH Bone turnover and mineral metabolism in adult patients with hypophosphatasia treated with asfotase alfa Seltene osteologische Erkrankungen und ihre Therapie Burden of Illness in Adults With Hypophosphatasia: Data From the Global Hypophosphatasia Patient Registry Diagnostik und Management der Hypophosphatasie Diagnostik und Management der Hypophosphatasie Die Hypophosphatasie im Erwachsenenalter : Charakterisierung des Krankheitsbildes und Etablierung therapeutischer Strategien Pediatric hypophosphatasia: lessons learned from a retrospective single-center chart review of 50 children Physical Function and Health‐Related Quality of Life in Adults Treated With Asfotase Alfa for Pediatric‐Onset Hypophosphatasia Bone mineral density and fracture risk in adult patients with hypophosphatasia Pediatric hypophosphatasia: lessons learned from a retrospective single-center chart review of 50 children Genetische Ursachen und Therapie der Osteogenesis imperfecta Therapie der Hypophosphatasie Von der Initiative (der Deutschen Gesellschaft für Osteologie [DGO]) zum Netzwerk: Vorstellung des deutschsprachigen Netzwerks für Seltene Osteopathien (NetsOs) Impact of whole-body vibration exercise on physical performance and bone turnover in patients with monoclonal gammopathy of undetermined significance Osteoporose: Oberstes Ziel ist die Vermeidung von Frakturen Subtrochanteric and diaphyseal femoral fractures in hypophosphatasia—not atypical at all Cellular pharmacodynamic effects of Pycnogenol\(^{®}\) in patients with severe osteoarthritis: a randomized controlled pilot study Distribution of constituents and metabolites of maritime pine bark extract (Pycnogenol\(^{®}\)) into serum, blood cells, and synovial fluid of patients with severe osteoarthritis: a randomized controlled trial Cellular pharmacodynamic effects of Pycnogenol® in patients with severe osteoarthritis: a randomized controlled pilot study The Transcriptional Profile of Mesenchymal Stem Cell Populations in Primary Osteoporosis Is Distinct and Shows Overexpression of Osteogenic Inhibitors A small scale cell culture system to analyze mechanobiology using reporter gene constructs and polyurethane dishes Ergebnisse nach operativ versorgten Frakturen des oberen Sprunggelenks

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Katalog der Deutschen Nationalbibliothek

Lothar Seefried (1976-)

XLH Matters 2024: expert insights and practical tools for enhancing care of people living with X-linked hypophosphataemia

Developing a Standardised Dataset for Natural History Studies in Fibrous Dysplasia/McCune-Albright Syndrome

Grading Pseudofractures—The “Breach–Beak–Bump–Bridge” Approach

Diagnosis and Treatment of Hypophosphatasia

Publisher Correction: Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia

XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes

Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia

Anticipated effects of burosumab treatment on long-term clinical sequelae in XLH: expert perspectives

Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults

Impact of muscular symptoms and/or pain on disease characteristics, disability, and quality of life in adult patients with hypophosphatasia: A cross-sectional analysis from the Global HPP Registry

Whole genome sequencing in adults with clinical hallmarks of hypophosphatasia negative for ALPL variants

Correction: Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults

Effectiveness of asfotase alfa for treatment of adults with hypophosphatasia: results from a global registry

Clinical Profiles of Children with Hypophosphatasia prior to Treatment with Enzyme Replacement Therapy: An Observational Analysis from the Global HPP Registry

Challenges in the management of tumor-induced osteomalacia (TIO)

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

Proposed diagnostic criteria for the diagnosis of hypophosphatasia in children and adolescents: results from the HPP International Working Group

The challenge of hypophosphatasia diagnosis in adults: results from the HPP International Working Group Literature Surveillance

Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults

XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH)

Efficacy of Zoledronic Acid in the Treatment of Nonmalignant Painful Bone Marrow Lesions: A Triple‐Blind, Randomized, Placebo‐Controlled Phase III Clinical Trial (ZoMARS)

Einfluss von Vibrationstraining auf körperliche Leistungsfähigkeit, Alltagsaktivität und Lebensqualität von Patienten mit monoklonaler Gammopathie

Supplement: Impaired Physical Performance in X-linked Hypophosphatemia is not caused by depleted muscular phosphate stores

Clinical profiles of treated and untreated adults with hypophosphatasia in the Global HPP Registry

Lower limb bone geometry in adult individuals with X-linked hypophosphatemia: an observational study

Feasibility of simple exercise interventions for men with osteoporosis – A prospective randomized controlled pilot study

Insuffizienzfraktur der Klavikula nach Implantation einer inversen Schulterendoprothese

Sarcopenia and Malnutrition Screening in Female Osteoporosis Patients — A Cross-Sectional Study

X-chromosomale Hypophosphatämie - Phosphatdiabetes - XLH

X-chromosomale Hypophosphatämie - Phosphatdiabetes - XLH

Bone turnover and mineral metabolism in adult patients with hypophosphatasia treated with asfotase alfa

Seltene osteologische Erkrankungen und ihre Therapie

Burden of Illness in Adults With Hypophosphatasia: Data From the Global Hypophosphatasia Patient Registry

Diagnostik und Management der Hypophosphatasie

Diagnostik und Management der Hypophosphatasie

Die Hypophosphatasie im Erwachsenenalter : Charakterisierung des Krankheitsbildes und Etablierung therapeutischer Strategien

Pediatric hypophosphatasia: lessons learned from a retrospective single-center chart review of 50 children

Physical Function and Health‐Related Quality of Life in Adults Treated With Asfotase Alfa for Pediatric‐Onset Hypophosphatasia

Bone mineral density and fracture risk in adult patients with hypophosphatasia

Pediatric hypophosphatasia: lessons learned from a retrospective single-center chart review of 50 children

Genetische Ursachen und Therapie der Osteogenesis imperfecta

Therapie der Hypophosphatasie

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

Impact of whole-body vibration exercise on physical performance and bone turnover in patients with monoclonal gammopathy of undetermined significance

Osteoporose: Oberstes Ziel ist die Vermeidung von Frakturen

Subtrochanteric and diaphyseal femoral fractures in hypophosphatasia—not atypical at all

Cellular pharmacodynamic effects of Pycnogenol\(^{®}\) in patients with severe osteoarthritis: a randomized controlled pilot study

Distribution of constituents and metabolites of maritime pine bark extract (Pycnogenol\(^{®}\)) into serum, blood cells, and synovial fluid of patients with severe osteoarthritis: a randomized controlled trial

Cellular pharmacodynamic effects of Pycnogenol® in patients with severe osteoarthritis: a randomized controlled pilot study

The Transcriptional Profile of Mesenchymal Stem Cell Populations in Primary Osteoporosis Is Distinct and Shows Overexpression of Osteogenic Inhibitors

A small scale cell culture system to analyze mechanobiology using reporter gene constructs and polyurethane dishes

Ergebnisse nach operativ versorgten Frakturen des oberen Sprunggelenks