G. Hoffmann
发表
J. Rothberg,
F. Polleux,
Tommy L. Lewis,
2016,
Cell reports.
G. Hoffmann,
G. Gramer,
J. Hennermann,
2021,
Molecular genetics and metabolism reports.
M. Sahin,
G. Hoffmann,
H. Jungbluth,
2016,
Brain : a journal of neurology.
C. Schaaf,
S. Uhrig,
D. Hübschmann,
2022,
bioRxiv.
Manuela Pendziwiat,
H. Muhle,
R. Møller,
2022,
Neurology: Genetics.
C. Marshall,
Birgit B Ertl-Wagner,
E. Mayatepek,
2022,
Clinical genetics.
M. Nöthen,
S. Mundlos,
T. Meitinger,
2022,
Deutsches Arzteblatt international.
S. Kölker,
J. Okun,
G. Hoffmann,
2022,
Molecular genetics and metabolism.
I. Harting,
M. Parker,
A. van Haeringen,
2021,
European Journal of Human Genetics.
C. Thiel,
K. Tsiakas,
S. Kölker,
2021,
Journal of inherited metabolic disease.
G. Rubboli,
R. Møller,
T. Bast,
2021,
International journal of molecular sciences.
C. Schwartz,
E. Bonora,
T. Pippucci,
2015,
Gene.
P. Scambler,
R. Surtees,
P. Clayton,
2005,
Human molecular genetics.
M. Verbeek,
N. Blau,
R. Artuch,
2017,
Orphanet Journal of Rare Diseases.
J. Köhrle,
M. Bertoldi,
U. Schweizer,
2012,
Molecular and Cellular Endocrinology.
Robert W. Taylor,
R. Durbin,
T. Wieland,
2015,
Annals of clinical and translational neurology.
W. Nyhan,
S. Kölker,
G. Hoffmann,
2017
.
M. Verbeek,
H. Goez,
J. Friedman,
2020,
Orphanet Journal of Rare Diseases.
B. Echenne,
N. Blau,
B. Thöny,
2006,
Pediatric neurology.
C. Salerno,
C. Crifó,
O. Sommerburg,
2003,
Free radical biology & medicine.
E. Mayatepek,
A. Schulze,
G. Hoffmann,
2002,
Clinica chimica acta; international journal of clinical chemistry.
G. Hoffmann,
S. Sauer,
M. Morath,
2008,
Biochimica et biophysica acta.
Thomas Meitinger,
Guy Lenaers,
Patrizia Amati-Bonneau,
2016,
American journal of human genetics.
F. Schaefer,
G. Hoffmann,
E. Wühl,
2011,
Circulation.
J. Okun,
G. Hoffmann,
P. Burgard,
2016,
JIMD reports.
A. Bener,
T. Ben-Omran,
J. Zschocke,
2010,
The Journal of pediatrics.
R. Badii,
A. Bener,
J. Zschocke,
2006,
Human mutation.
M. Baumgartner,
S. Almashanu,
T. Suormala,
2004,
American journal of human genetics.
E. Bertini,
M. Simpson,
H. Goebel,
2012,
Nature Genetics.
S. Kölker,
G. Hoffmann,
Matthias Zielonka,
2020,
Journal of inherited metabolic disease.
K. Weiss,
S. Kölker,
G. Hoffmann,
2022,
Nutrients.
A. Hamann,
P. Nawroth,
S. Lichtenstein,
2011,
International journal of endocrinology.
A. Hamann,
P. Nawroth,
S. Lichtenstein,
2011
.
E. Mayatepek,
S. Kölker,
G. Hoffmann,
2002,
Neuropediatrics.
D. Zafeiriou,
B. Weschke,
A. Mégarbané,
2010,
Brain : a journal of neurology.
R. Wevers,
L. Heuvel,
G. Hoffmann,
2000,
Annals of human genetics.
M. Naumann,
R. Wevers,
G. Hoffmann,
2003,
Annals of neurology.
K. Scheffler,
D. Berg,
A. Padovani,
2020,
Neurology.
S. Kins,
S. Kölker,
J. Okun,
2006,
Pediatric Research.
I. Harting,
P. Bachert,
E. Mayatepek,
2003,
Annals of neurology.
E. Mayatepek,
F. Fresser,
G. Utermann,
2000,
Human Genetics.
G. Hoffmann,
M. Ries,
K. Mechler,
2015,
Genetics in Medicine.
I. Harting,
J. Zschocke,
S. Kölker,
2009,
Brain : a journal of neurology.
N. Blau,
R. Artuch,
À. García‐Cazorla,
2020,
Journal of inherited metabolic disease.
M. Carl,
I. Harting,
T. Meitinger,
2016,
American journal of human genetics.
N. Hübner,
F. Spagnoli,
N. Blau,
2014,
Diabetes.
N. Hübner,
F. Spagnoli,
N. Blau,
2014
.
M. Muckenthaler,
A. Schulz,
D. Hübschmann,
2017,
Clinical immunology.
M. Baumgartner,
I. Harting,
B. Plecko,
2022,
Journal of inherited metabolic disease.
I. Harting,
C. Greenberg,
J. Zschocke,
2017,
Journal of Inherited Metabolic Disease.
S. Listl,
S. Kölker,
G. Hoffmann,
2013,
Orphanet Journal of Rare Diseases.
M. Durán,
C. Greenberg,
E. Christensen,
2011,
Journal of Inherited Metabolic Disease.
I. Harting,
J. Zschocke,
S. Kölker,
2010,
Annals of neurology.
J. Zschocke,
S. Kölker,
G. Hoffmann,
2007,
Pediatric Research.
C. Harding,
S. Kölker,
J. Okun,
2006,
Journal of neurochemistry.
I. Harting,
O. Bodamer,
J. Zschocke,
2005,
Neurology.
S. Kölker,
J. Okun,
G. Hoffmann,
2005,
Journal of Biological Chemistry.
P. Guldberg,
J. Zschocke,
G. Hoffmann,
2000,
Journal of medical genetics.
S. Kölker,
J. Okun,
G. Hoffmann,
2011,
Brain : a journal of neurology.
J. Smeitink,
L. P. Van den Heuvel,
D. Rating,
2005,
Clinical chemistry.
D. Zafeiriou,
G. Horvath,
G. Hoffmann,
2022,
Annals of neurology.
P. Guldberg,
I. Dianzani,
V. Romano,
1998,
American journal of human genetics.
G. Hoffmann,
M. Ries,
Anette Lampert,
2016,
PloS one.
W. Oertel,
J. C. Möller,
O. Bandmann,
2004,
Movement disorders : official journal of the Movement Disorder Society.
W. Oertel,
J. C. Möller,
O. Bandmann,
2004
.
D. Zafeiriou,
H. Goez,
J. Friedman,
2021,
Journal of inherited metabolic disease.
S. Kölker,
G. Hoffmann,
Matthias Zielonka,
2019,
Genetics in Medicine.
A. Ziegler,
S. Kölker,
G. Hoffmann,
2020,
Neuropediatrics.
G. Hoffmann,
M. Lindner,
P. Burgard,
2013,
Molecular genetics and metabolism.
C. Klein,
G. Hoffmann,
N. Wolf,
2011,
Movement disorders : official journal of the Movement Disorder Society.
R. Rossi,
J. Zeman,
S. Kmoch,
2007,
The Journal of pediatrics.
K. Unsicker,
E. Mayatepek,
S. Kölker,
2002,
The Journal of Biological Chemistry.
B. Burton,
M. Yudkoff,
Aneal Khan,
2016,
Molecular genetics and metabolism.
A. Ziegler,
O. Witt,
M. Gorenflo,
2019,
Orphanet Journal of Rare Diseases.
Amrish Kumar,
J. Probst,
S. Kölker,
2020,
Experimental Neurology.
G. Engelmann,
G. Hoffmann,
E. Wühl,
2012,
European Journal of Pediatrics.
G. Hoffmann,
D. Haas,
G. Hoffmann,
2006,
Orphanet journal of rare diseases.
H. Bremer,
E. Mayatepek,
G. Hoffmann,
1993,
The Journal of pediatrics.
G. Hoffmann,
M. Bettendorf,
Laura Henn,
2019,
Journal of clinical research in pediatric endocrinology.
M. Weigand,
U. Felderhoff-Müser,
G. Hoffmann,
2021,
Medicine.
R. Wanders,
E. Mayatepek,
J. Zschocke,
2000,
Pediatric Research.
Martin Lindner,
E. Mayatepek,
A. Schulze,
2003,
Pediatrics.
P. Vreken,
A. V. van Kuilenburg,
M. Spraul,
2001,
Magnetic resonance in medicine.
N. Blau,
J. Okun,
G. Hoffmann,
2010,
Journal of Inherited Metabolic Disease.
R. Surtees,
S. Heales,
G. Hoffmann,
2002,
Pediatric Research.
E. Mayatepek,
L. Ijlst,
R. Wanders,
2001,
Journal of the Neurological Sciences.
T. Meitinger,
T. Strom,
H. Prokisch,
2018,
American journal of human genetics.
G. Hoffmann,
G. Gramer,
G. Hoffmann,
2020,
Current Medical Science.
Michaela Frye,
Richard Durbin,
Holger Prokisch,
2016,
Nature Communications.
D. Russell,
G. Engelmann,
P. Clayton,
2012,
World journal of gastroenterology.
Thomas Meitinger,
Julien Gagneur,
Holger Prokisch,
2015,
American journal of human genetics.
T. Wieland,
T. Meitinger,
T. Strom,
2012,
Journal of Medical Genetics.
Rafael A. Tesorero,
J. Okun,
G. Hoffmann,
2023,
PloS one.
A. Schulz,
S. Ehl,
R. Krüger,
2023,
Journal of Clinical Immunology.
German newborn screening for Cystic fibrosis: Parental perspectives and suggestions for improvements
O. Sommerburg,
I. Brockow,
G. Hoffmann,
2022,
Pediatric pulmonology.
M. Godejohann,
S. Kölker,
J. Okun,
2022,
Clinical biochemistry.
C. Schaaf,
S. Kölker,
G. Hoffmann,
2022,
Medizinische Genetik.
M. Muckenthaler,
O. Sommerburg,
A. Kulozik,
2021,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
S. Grünert,
S. Kölker,
J. Okun,
2021,
The Journal of pediatrics.
S. Grünert,
T. Marquardt,
S. Kölker,
2021,
Journal of inherited metabolic disease.
M. Leichsenring,
S. Grünert,
S. Kölker,
2020,
Pediatrics.
K. Weiss,
J. Okun,
R. Posset,
2019,
The Journal of pediatrics.
Dong Hwan Lee,
Nguyen Ngoc Khanh,
T. Taketani,
2018,
Molecular genetics and metabolism reports.
T. Ben-Omran,
J. Okun,
G. Hoffmann,
2017,
World Journal of Pediatrics.
J. Loeber,
M. Cornel,
S. Kölker,
2016,
JIMD reports.
A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document
Domenica Taruscio,
Luciano Vittozzi,
Kathrin Rupp,
2013,
European Journal of Human Genetics.
M. Baumgartner,
R. Fingerhut,
S. Kölker,
2017,
PloS one.
V. Stoppioni,
J. Vockley,
B. Burton,
2020,
American journal of human genetics.
D. Matern,
G. Hoffmann,
M. Lindner,
2010,
Journal of Inherited Metabolic Disease.
A. Gropman,
J. Probst,
S. Kölker,
2020,
Molecular genetics and metabolism.
A. Gropman,
S. Kölker,
R. Posset,
2019,
Annals of clinical and translational neurology.
J. Okun,
G. Hoffmann,
P. Feyh,
2018,
World Journal of Pediatrics.
Edward L. Huttlin,
J. Mullikin,
T. Meitinger,
2017,
American journal of human genetics.
M. Leichsenring,
G. Hoffmann,
M. Lindner,
2011,
Orphanet journal of rare diseases.
O. Sommerburg,
M. Macek,
J. Hammermann,
2016,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
M. Muckenthaler,
M. Gahr,
O. Sommerburg,
2015,
Pediatric pulmonology.
M. Muckenthaler,
O. Sommerburg,
A. Kulozik,
2010,
Journal of Inherited Metabolic Disease.
M. Muckenthaler,
M. Gahr,
O. Sommerburg,
2014,
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
N. Blau,
G. Hoffmann,
G. Hoffmann,
1998,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
U. Langenbeck,
G. Hoffmann,
P. Heidemann,
1982,
European Journal of Pediatrics.
G. Hoffmann,
K. Hinderhofer,
M. Ries,
2017,
Journal of Inherited Metabolic Disease.
S. Kölker,
G. Hoffmann,
Matthias Zielonka,
2017,
Genetics in Medicine.
R. Dittmann,
G. Hoffmann,
M. Ries,
2017,
International journal of methods in psychiatric research.
E. Mayatepek,
G. Hoffmann,
G. Hoffmann,
1995,
Pediatric Research.
G. Matthijs,
C. Thiel,
Kristen Hanson,
2012,
Human mutation.
M. Schlesner,
G. Rappold,
G. Hoffmann,
2020,
Hormone Research in Paediatrics.
J. van Reeuwijk,
L. Hoefsloot,
H. van Bokhoven,
2010,
Brain : a journal of neurology.
E. Berger,
K. von Figura,
C. Thiel,
2002,
The Journal of clinical investigation.
T. Bast,
C. Schaaf,
T. Haack,
2021,
Human mutation.
G. Hoffmann,
M. Ries,
Anette Lampert,
2016,
Orphanet Journal of Rare Diseases.
H. Bremer,
K. Gibson,
W. Nyhan,
2005,
European Journal of Pediatrics.
D. Bhugra,
A. Bener,
G. Hoffmann,
2017,
Annals of African medicine.
M. Carl,
S. Kölker,
J. Okun,
2019,
PloS one.
T. Wieland,
T. Meitinger,
T. Strom,
2014,
Molecular genetics and metabolism.
H. Prokisch,
Ryan J Schulze,
M. McNiven,
2019,
American journal of human genetics.
R. Hell,
P. Nawroth,
G. Hoffmann,
2021,
International journal of molecular sciences.
M. Becker,
M. Freichel,
M. Hecker,
2020,
International journal of molecular sciences.
D. Zafeiriou,
M. Verbeek,
H. Goez,
2021,
Nature Communications.
S. Naidu,
G. Scheper,
C. Proud,
2003,
American journal of human genetics.
A. Ziegler,
J. Denecke,
I. Sinning,
2019,
Human mutation.
H. Möller,
P. Guldberg,
J. Denecke,
2001,
Pediatric Research.
E. Mayatepek,
J. Jaeken,
G. Hoffmann,
2001,
Neuropediatrics.
G. Hoffmann,
P. Burgard,
C. Langhans,
2016,
Prostaglandins, leukotrienes, and essential fatty acids.
C. Fischer,
T. Ben-Omran,
J. Zschocke,
2009,
Human mutation.
F. Rivier,
B. Echenne,
G. Hoffmann,
2008,
Epileptic disorders : international epilepsy journal with videotape.
G. Hoffmann,
M. Ries,
J. Döring,
2016,
PloS one.
E. Mayatepek,
B. Liebl,
R. von Kries,
2004,
European Journal of Pediatrics.
G. Kochs,
R. Bartenschlager,
T. Iftner,
2021,
JAMA pediatrics.
S. Kölker,
G. Hoffmann,
D. Ebrahimi-Fakhari,
2017,
Journal of Inherited Metabolic Disease.
A. Schulze,
J. Okun,
G. Hoffmann,
2014,
Gene.
A. Bener,
G. Hoffmann,
G. Hoffmann,
2010,
International journal of pediatric endocrinology.
P. Striano,
U. Stephani,
P. Bauer,
2012,
Human mutation.
P. Schirmacher,
H. Bartsch,
G. Engelmann,
2015,
Hepatobiliary surgery and nutrition.
P. Broser,
Birgit Stark,
H. Muhle,
2020,
Biomedicines.
R. Durbin,
T. Meitinger,
T. Strom,
2016,
American journal of human genetics.
M. Carl,
J. Probst,
S. Kölker,
2019,
Experimental Neurology.
M. Carl,
S. Kölker,
J. Okun,
2018,
PloS one.
J. Rosenfeld,
J. Lupski,
D. Horn,
2020,
Genetics in Medicine.
R. Russell,
H. Prokisch,
C. Klein,
2019,
Genetics in Medicine.
Robert W. Taylor,
I. Harting,
T. Meitinger,
2018,
Genetics in Medicine.
Robert W. Taylor,
T. Wieland,
I. Harting,
2016,
Journal of Inherited Metabolic Disease.
S. Kranig,
B. Toenshoff,
G. Hoffmann,
2018,
BMJ Open.
G. Hoffmann,
M. Ries,
Thomas Breil,
2018,
BMJ Open.
G. Hoffmann,
M. Ries,
Thomas Breil,
2016,
PloS one.
E. van Binsbergen,
W. Dobyns,
N. Matsumoto,
2017,
Brain : a journal of neurology.
H. Lehr,
K. Gibson,
G. Hoffmann,
1993,
Pediatric Research.
G. Hoffmann,
P. Feyh,
G. Hoffmann,
2003
.
S. Kölker,
G. Hoffmann,
S. Garbade,
2020,
Genetics in Medicine.
G. Hoffmann,
M. Ries,
K. Mechler,
2015,
Orphanet Journal of Rare Diseases.
H. Lauffer,
P. Lauenstein,
G. Seidlitz,
2015,
Neuropediatrics.
R. Eils,
M. Carl,
S. Wiemann,
2018,
Molecular genetics and metabolism.
S. Kölker,
G. Hoffmann,
G. Hoffmann,
2013,
Handbook of clinical neurology.
S. Kölker,
G. Hoffmann,
G. Hoffmann,
2012
.
J. Valk,
H. Hartung,
M. Durán,
1992,
Annals of neurology.
W. Oertel,
B. Tackenberg,
J. C. Möller,
2007,
Movement disorders : official journal of the Movement Disorder Society.
G. Engelmann,
G. Hoffmann,
U. Teufel,
2014,
Hepatitis monthly.
F. Gabreëls,
R. Wevers,
J. Smeitink,
1999,
Journal of Inherited Metabolic Disease.
A. Bener,
G. Hoffmann,
A. A. Wahab,
2006,
Birth defects research. Part A, Clinical and molecular teratology.
V. Pawlak,
E. Mayatepek,
G. Köhr,
2002,
The European journal of neuroscience.
A. Bener,
G. Hoffmann,
M. Al-Ali,
2009,
Minerva pediatrica.
A. Bener,
G. Hoffmann,
M. Darwish,
2013
.
A. Bener,
G. Hoffmann,
M. Al-Ali,
2009,
International journal of food sciences and nutrition.
N. Blau,
C. Thiel,
J. Okun,
2016,
Molecular genetics and metabolism.
G. Hoffmann,
E. Wühl,
J. Schenk,
2017,
Medical ultrasonography.
S. Kölker,
G. Hoffmann,
S. Garbade,
2020,
Genetics in medicine : official journal of the American College of Medical Genetics.
M. Durán,
M. Knaap,
D. Rabier,
1999,
Journal of Inherited Metabolic Disease.
D. Souza,
M. Wajner,
C. Ribeiro,
2004,
Neurochemistry International.
S. Kölker,
J. Okun,
G. Hoffmann,
2004,
Annals of neurology.
V. Pawlak,
E. Mayatepek,
G. Köhr,
2002
.
M. Wajner,
E. Mayatepek,
B. Ahlemeyer,
2001,
Brain Research.
J. Zschocke,
G. Hoffmann,
G. Hoffmann,
1999,
Journal of Inherited Metabolic Disease.
B. Ahlemeyer,
J. Krieglstein,
S. Kölker,
1999,
Journal of Inherited Metabolic Disease.
J. Zschocke,
W. Buckel,
M. Liesert,
1999,
Journal of Inherited Metabolic Disease.
G. Hoffmann,
R. Forstner,
J. Tröger,
1999,
Pediatric Radiology.
W Lehnert,
M. Durán,
E. Christensen,
1996,
Neuropediatrics.
G. Hoffmann,
G. Hoffmann,
2000
.
W. Chan,
H. Prokisch,
F. Alkuraya,
2017,
Human mutation.
J. Hoheisel,
N. Blau,
Christian Betzen,
2016,
Scientific Reports.
A. Ziegler,
M. Weiler,
A. Ziegler,
2019,
Der Nervenarzt.
T. Wieland,
T. Meitinger,
T. Strom,
2012,
American journal of human genetics.
E. Sistermans,
M. McDonald,
T. Ben-Omran,
2013,
American journal of human genetics.
G. Hoffmann,
Matthias Zielonka,
S. Garbade,
2020,
PloS one.
S. Kölker,
G. Hoffmann,
Matthias Zielonka,
2018,
Genetics in Medicine.
S. Kölker,
G. Hoffmann,
Matthias Zielonka,
2017,
Genetics in Medicine.
K. Gibson,
G. Hoffmann,
R. Keller,
1997,
Pediatric Research.
T. Giese,
H. Prokisch,
C. Klein,
2021,
Journal of Clinical Immunology.
E. Mayatepek,
B. Ahlemeyer,
J. Krieglstein,
2001,
Journal of neuroscience research.
H. Karch,
B. Tönshoff,
Christian Betzen,
2018,
American journal of physiology. Renal physiology.
T. Bast,
S. Kölker,
G. Hoffmann,
2020,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
B. Ahlemeyer,
J. Krieglstein,
S. Kölker,
2003,
Neurochemistry International.
O. Linderkamp,
E. Mayatepek,
A. Schulze,
2002,
Pediatric Research.
W. Nyhan,
J. Zschocke,
F. Hoffmann,
2021,
Encyclopedia of Autism Spectrum Disorders.
M. Gorenflo,
S. Kölker,
G. Hoffmann,
2022,
Molecular genetics and metabolism.
S. Kölker,
G. Hoffmann,
D. Ebrahimi-Fakhari,
2014,
Pediatric Research.
K. Kavanagh,
R. Wanders,
C. Bartram,
2010,
EMBO molecular medicine.
M. Baumgartner,
Á. Schuler,
N. Blau,
2008,
Molecular genetics and metabolism.
Robert W. Taylor,
A. Ballabio,
E. Bertini,
2020,
Journal of inherited metabolic disease.
S. Grünert,
G. Hoffmann,
B. Stiller,
2020,
Orphanet Journal of Rare Diseases.
R. Rodenburg,
J. Smeitink,
L. P. Van den Heuvel,
2006,
The Biochemical journal.
J. Motsch,
G. Hoffmann,
M. Bernhard,
2009,
Deutsches Arzteblatt international.
B. Tönshoff,
Bettina Hoppe,
G. Hoffmann,
2019,
BMC Research Notes.
N. Blau,
G. Hoffmann,
Matthias Zielonka,
2015,
JIMD reports.
B. Schoser,
G. Hoffmann,
P. Smit,
2015,
Journal of Inherited Metabolic Disease.
G. Hoffmann,
F. Hörster,
G. Hoffmann,
2004,
Pediatric Nephrology.
G. Hoffmann,
G. Hoffmann,
2018
.
N. Blau,
G. Hoffmann,
T. Opladen,
2012,
Journal of Inherited Metabolic Disease.
D. Berg,
M. Spraul,
A. Pilotto,
2020,
Orphanet Journal of Rare Diseases.