F. Rutsch
发表
W. Schwindt,
G. Nürnberg,
P. Nürnberg,
2010,
Human mutation.
K. Langer,
F. Rutsch,
J. Keuth,
2020,
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
R. Terkeltaub,
F. Rutsch,
Y. Nitschke,
2011,
Journal of cellular and molecular medicine.
W. Greiner,
F. Rutsch,
F. Trefz,
2021,
Molecular genetics and metabolism reports.
C. Lohmann,
J. Bertrand,
T. Pap,
2020,
Annals of the Rheumatic Diseases.
Y. Crow,
G. Rice,
I. Buers,
2017,
Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.
F. Rutsch,
Y. Nitschke,
2017,
Current Osteoporosis Reports.
I. Buers,
F. Rutsch,
Y. Nitschke,
2016
.
I. Buers,
F. Rutsch,
Y. Nitschke,
2016,
Cytokine & growth factor reviews.
A. Toutain,
F. Schliess,
D. Häussinger,
2006,
Journal of Inherited Metabolic Disease.
F. Ebinger,
F. Rutsch,
H. Klünemann,
2011,
Monatsschrift Kinderheilkunde.
V. Müller,
E. Pogatzki-Zahn,
A. Vanlander,
2019,
Muscle & nerve.
F. Rutsch,
J. Weglage,
R. Feldmann,
2017,
Acta paediatrica.
F. Rutsch,
Y. Nitschke,
2012,
Trends in cardiovascular medicine.
G. Leftheriotis,
A. Sicard,
F. Rutsch,
2020,
Frontiers in Cell and Developmental Biology.
W. Greiner,
F. Rutsch,
A. Muntau,
2019,
Orphanet Journal of Rare Diseases.
K. Wernecke,
P. Peters,
F. Rutsch,
1991,
Radiology.
G. Leftheriotis,
V. Macrae,
A. Váradi,
2016,
Current opinion in pharmacology.
R. Terkeltaub,
A. Sinaiko,
T. Roscioli,
2003,
Nature Genetics.
Y. Wada,
H. Omran,
K. Boycott,
2015,
American journal of human genetics.
J. Winkler,
A. Ferbert,
G. Schuierer,
2015,
Orphanet Journal of Rare Diseases.
V. Macrae,
F. Rutsch,
C. Huesa,
2012,
Bone.
V. Macrae,
F. Rutsch,
C. Huesa,
2012,
Bone.
A. V. van Kuilenburg,
L. Zoetekouw,
H. van Lenthe,
2004,
Human molecular genetics.
G. Zampino,
A. Angius,
L. Crisponi,
2016,
American journal of human genetics.
M. McCulloch,
R. Terkeltaub,
N. Chassaing,
2012,
American journal of human genetics.
A. Toutain,
F. Schliess,
D. Häussinger,
2005,
The New England journal of medicine.
B. Bembi,
N. Ruf,
F. Rutsch,
2006,
European Journal of Pediatrics.
N. Ruf,
Shuan-Pei Lin,
F. Rutsch,
2005,
American journal of medical genetics. Part A.
R. Terkeltaub,
P. Nürnberg,
B. Uhlenberg,
2005,
Human mutation.
P. Schauerte,
R. Terkeltaub,
I. Goldfine,
2001,
The American journal of pathology.
R. Terkeltaub,
T. Strom,
P. Nürnberg,
2008,
Circulation. Cardiovascular genetics.
T. Marquardt,
M. du Moulin,
F. Rutsch,
2014,
JIMD reports.
F. Rutsch,
2018,
EBioMedicine.
P. Heuschmann,
D. Lorenz,
M. de Greck,
2021,
Orphanet Journal of Rare Diseases.
W. Gahl,
C. Ferreira,
G. Khursigara,
2021,
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
Kristina W. Kintziger,
Yan Yan,
I. Buers,
2018,
Experimental & Molecular Medicine.
F. Rutsch,
Y. Nitschke,
2012,
Front. Gene..
N. Chassaing,
L. Schurgers,
F. Rutsch,
2010,
American journal of medical genetics. Part A.
Kocuria rhizophila Adds to the Emerging Spectrum of Micrococcal Species Involved in Human Infections
T. Marquardt,
K. Becker,
G. Peters,
2008,
Journal of Clinical Microbiology.
I. Salusky,
B. Gales,
F. Rutsch,
2021,
Genetics in Medicine.
B. Mallick,
L. Crisponi,
F. Rutsch,
2010,
Developmental medicine and child neurology.
C. Baerwald,
K. Parhofer,
F. Rutsch,
2020,
Annals of Nutrition and Metabolism.
J. Burgerhof,
S. Huijbregts,
F. Rutsch,
2021,
Pediatric Research.
M. Baumgartner,
T. Suormala,
G. Nürnberg,
2009,
Nature Genetics.
P. Pennekamp,
B. Skryabin,
I. Buers,
2016,
Journal of cellular and molecular medicine.
T. Suormala,
F. Rutsch,
B. Fowler,
2011,
Journal of Inherited Metabolic Disease.
P. Nürnberg,
B. Gasnier,
F. Rutsch,
2010,
Journal of Molecular Medicine.
T. Suormala,
P. Nürnberg,
M. Toliat,
2010,
Journal of Inherited Metabolic Disease.
S. Terry,
J. Uitto,
Qiaoli Li,
2022,
PLoS genetics.
M. Baumgartner,
M. Hochuli,
R. Lachmann,
2013,
Journal of Inherited Metabolic Disease.
C. Ferreira,
F. Rutsch,
M. Kiel,
2022,
Orphanet Journal of Rare Diseases.
C. Ferreira,
G. Khursigara,
F. Rutsch,
2022,
Human mutation.
G. Khursigara,
F. Rutsch,
Y. Nitschke,
2021,
The Journal of clinical endocrinology and metabolism.
A. Federico,
C. V. van Karnebeek,
C. Hollak,
2018,
Orphanet Journal of Rare Diseases.
F. Eyskens,
A. Burlina,
V. Leuzzi,
2021,
Orphanet Journal of Rare Diseases.
R. König,
V. Simon,
A. Fernández-Sesma,
2011,
PLoS pathogens.
Nan Yan,
T. Fujita,
M. Takami,
2022,
Journal of immunology.
C. Lohmann,
J. Bertrand,
T. Pap,
2009,
Arthritis and rheumatism.
D. Sillence,
T. Roscioli,
F. Rutsch,
2009,
Nature Clinical Practice Endocrinology &Metabolism.
L. Corvaglia,
G. Faldella,
F. Rutsch,
2011,
JIMD reports.
D. Sillence,
T. Roscioli,
F. Rutsch,
2009,
Nature Reviews Endocrinology.
R. Terkeltaub,
F. Rutsch,
Y. Nitschke,
2011,
Circulation research.
S. Grünert,
J. Sass,
G. Mitchell,
2017,
Molecular Genetics and Metabolism.
W. Böcker,
P. Peters,
F. Rutsch,
1998,
Pediatric Radiology.
R. König,
D. Elleder,
R. Sachidanandam,
2016,
Retrovirology.
C. V. van Karnebeek,
M. Stojiljkovic,
P. Mathisen,
2019,
Nutrients.
R. König,
F. Lasitschka,
E. Flory,
2012,
Nature Medicine.
F. Rutsch,
J. Weglage,
R. Feldmann,
2019,
Molecular genetics and metabolism.
H. Möller,
B. Koletzko,
T. Marquardt,
2013,
Molecular genetics and metabolism.
G. Chabot,
F. Rutsch,
Y. Nitschke,
2011,
European Journal of Pediatrics.
E. Shoubridge,
M. Baumgartner,
T. Suormala,
2012,
Nature Genetics.
Y. Crow,
P. Nürnberg,
M. du Moulin,
2011,
Proceedings of the National Academy of Sciences.
D. Baker,
A. Brady,
Diana S. Johnson,
2020,
American journal of medical genetics. Part A.
L. Crisponi,
I. Buers,
F. Rutsch,
2022,
International journal of molecular sciences.
J. Charrow,
M. Irving,
K. White,
2020,
Journal of the Endocrine Society.
J. Charrow,
M. Irving,
K. White,
2020,
The Lancet.
J. Charrow,
M. Irving,
K. White,
2022,
Genetics in medicine : official journal of the American College of Medical Genetics.
J. Charrow,
M. Irving,
K. White,
2021,
Genetics in Medicine.
I. Buers,
F. Rutsch,
W. Höhne,
2016,
Human mutation.
P. Schauerte,
F. Rutsch,
H. Kalhoff,
2000,
Acta paediatrica.
G. Leftheriotis,
F. Rutsch,
Ludovic Martin,
2018,
Joint, bone, spine : revue du rhumatisme.
G. Ferrero,
A. Pucci,
F. Rutsch,
2009,
Acta paediatrica.
G. Leftheriotis,
V. Macrae,
T. Arányi,
2019,
Front. Cardiovasc. Med..
F. Rutsch,
Y. Nitschke,
G. Weissen-Plenz,
2008,
Advances in clinical chemistry.
Robert W. Taylor,
W. Chung,
H. Prokisch,
2017,
Annals of neurology.
Kristina W. Kintziger,
Yan Yan,
I. Buers,
2018,
Experimental & Molecular Medicine.
R. Terkeltaub,
F. Rutsch,
2005,
Joint, bone, spine : revue du rhumatisme.
R. Terkeltaub,
F. Rutsch,
2003,
Current opinion in rheumatology.
I. Buers,
F. Rutsch,
Y. Nitschke,
2020,
Arteriosclerosis, thrombosis, and vascular biology.
G. Leftheriotis,
G. Kauffenstein,
N. Navasiolava,
2019,
The British journal of dermatology.
S. Kölker,
R. Santer,
P. Burgard,
2022,
Journal of inherited metabolic disease.
A. Mottok,
F. Rutsch,
F. Louwen,
2009,
Fetal Diagnosis and Therapy.
M. Baumgartner,
M. Konrad,
J. Koenig,
2015,
Pediatric Nephrology.
R. König,
M. Emerman,
G. Lenzi,
2017
.
R. Hennekam,
Y. Crow,
P. Nürnberg,
2015,
American journal of human genetics.
P. Nürnberg,
Leonid Kalichman,
N. Ruf,
2005,
Arthritis research & therapy.
G. Usala,
B. Kamien,
A. Zankl,
2014,
Human mutation.
H. Omran,
A. Röpke,
L. Crisponi,
2020,
Stem cell research.
Crisponi/cold‐induced sweating syndrome: Differential diagnosis, pathogenesis and treatment concepts
G. Zampino,
L. Crisponi,
I. Buers,
2019,
Clinical genetics.
G. Zampino,
L. Crisponi,
M. Deiana,
2011,
European Journal of Human Genetics.
Robert Kleta,
Bernd Wollnik,
G. Usala,
2007,
American journal of human genetics.
M. Baumgartner,
S. Grünert,
S. Kölker,
2021,
Scientific Reports.
Ellen F. Macnamara,
E. Chew,
E. Dikoglu,
2020,
Genetics in Medicine.
H. Seifarth,
F. Rutsch,
Y. Nitschke,
2009,
Journal of cellular and molecular medicine.
F. Rutsch,
2015,
The British journal of dermatology.
F. Dell’Accio,
M. Schäfers,
J. Bertrand,
2012,
Annals of the rheumatic diseases.
R. Hennekam,
A. Feigenbaum,
J. Kleinheinz,
2013,
American journal of medical genetics. Part A.
U. Kornak,
C. Grasemann,
K. Sinningen,
2021,
Bone.
A. V. van Kuilenburg,
R. Wevers,
A. Ribes,
2006,
Nucleosides, nucleotides & nucleic acids.
F. Muntoni,
F. Cucca,
A. Fry,
2019,
Clinical genetics.
A. Busch,
I. Buers,
I. Kurth,
2017,
Clinical genetics.
F. Muntoni,
F. Cucca,
A. Fry,
2019
.
G. Zampino,
A. Angius,
L. Crisponi,
2018,
American journal of human genetics.
F. Rutsch,
J. Weglage,
R. Feldmann,
2018,
Acta paediatrica.
K. Parhofer,
F. Rutsch,
Christian Heimbold,
2023,
Molecular genetics and metabolism.
F. Rutsch,
Y. Nitschke,
Dayakar Seetha,
2012,
Journal of cardiovascular disease research.
A. Siddiqui,
N. Dlamini,
M. Splitt,
2009,
American journal of medical genetics. Part A.
F. Rutsch,
Y. Nitschke,
Dayakar Seetha,
2014
.
G. Ferrero,
A. Pucci,
F. Rutsch,
2009
.
R. Terkeltaub,
P. Nürnberg,
B. Uhlenberg,
2005
.
Sebastian A. Wagner,
R. König,
D. Elleder,
2016,
Retrovirology.
B. Burton,
C. Harding,
R. Zori,
2019,
Molecular genetics and metabolism.
A. Burlina,
F. Rutsch,
F. Trefz,
2015,
JIMD reports.
R. König,
D. Steinemann,
F. Rutsch,
2020,
Stem cell research.
G. Leftheriotis,
V. Macrae,
T. Arányi,
2019
.
J. Sass,
F. Rutsch,
S. Rust,
2017,
Journal of pediatric endocrinology & metabolism : JPEM.
E. Shoubridge,
M. Baumgartner,
T. Suormala,
2012,
Nature Genetics.
R. Terkeltaub,
T. Strom,
P. Nürnberg,
2008,
Circulation. Cardiovascular genetics.
F. Rutsch,
Y. Nitschke,
Zhiliang Cheng,
2024,
Cells.