Works by Hoffmann, G.

Results: 494

Combined methotrexate and high-dose vincristine chemotherapy with radiation therapy for small cell bronchogenic carcinoma.

Published in:

1985

By:

Holoye, Paul Y.;
Libnoch, Joseph A.;
Anderson, Tom;
Cox, James D.;
Byhardt, Roger W.;
Hoffmann, Raymond G.;
Holoye, P Y;
Libnoch, J A;
Anderson, T;
Cox, J D;
Byhardt, R W;
Hoffmann, R G

Publication type:

journal article

Urinary oxalate excretion increases with body size and decreases with increasing dietary calcium intake among healthy adults.

Published in:

1996

By:

Lemann Jr., Jacob;
Pleuss, Joan A.;
Worcester, Elaine M.;
Hornick, Laurel;
Schrab, Debra;
Hoffmann, Raymond G.;
Lemann, J Jr;
Pleuss, J A;
Worcester, E M;
Hornick, L;
Schrab, D;
Hoffmann, R G

Publication type:

journal article

Plasma leptin and insulin levels in weight-reduced obese women with normal body mass index: relationships with body composition and insulin.

Published in:

1999

By:

Guven, Safak;
El-Bershawi, Ahmed;
Sonnenberg, Gabriele E.;
Wilson, Charles R.;
Hoffmann, Raymond G.;
Krakower, Glenn R.;
Kissebah, Ahmed H.;
Guven, S;
El-Bershawi, A;
Sonnenberg, G E;
Wilson, C R;
Hoffmann, R G;
Krakower, G R;
Kissebah, A H

Publication type:

journal article

Relationship of distance from a radiotherapy facility and initial breast cancer treatment.

Published in:

2001

By:

Nattinger, Ann Butler;
Kneusel, Ronald T.;
Hoffmann, Raymond G.;
Gilligan, Mary Ann;
Nattinger, A B;
Kneusel, R T;
Hoffmann, R G;
Gilligan, M A

Publication type:

journal article

Impact of the Zinc Antiviral Protein on the Genomic Composition of RNA Viruses Infecting Vertebrates Open Access.

Published in:

Molecular Biology & Evolution, 2025, v. 42, n. 6, p. 1, doi. 10.1093/molbev/msaf135

By:

Simón, Diego;
Megrian, Daniela;
Walt, Hunter K;
Moreno, Pilar;
Musto, Héctor;
Hoffmann, Federico G;
Moratorio, Gonzalo

Publication type:

Article

Learning from people, things, and signs.

Published in:

Studies in Philosophy & Education, 2007, v. 26, n. 3, p. 185, doi. 10.1007/s11217-007-9027-5

By:

Hoffmann, Michael H. G.

Publication type:

Article

The αD-Globin Gene Originated via Duplication of an Embryonic α-Like Globin Gene in the Ancestor of Tetrapod Vertebrates.

Published in:

Molecular Biology & Evolution, 2007, v. 24, n. 9, p. 1982, doi. 10.1093/molbev/msm127

By:

Hoffmann, Federico G.;
Storz, Jay F.

Publication type:

Article

Die neueren Arzeneimittel. Für Apotheker, Ärzte und Drogisten bearbeitet von Dr. Bernhard Fischer Mit in den Text gedruckten Holzschnitten. Vierte vermehrte Auflage. Berlin, Verlag von Julius Springer. Preis 6 Mark.

Published in:

Archiv der Pharmazie, 1889, v. 227, n. 21, p. 1008, doi. 10.1002/ardp.18892272108

By:

Hoffmann, G.

Publication type:

Article

Commentar zur Pharmacopoea Germanica editio altera. Herausgeben von Dr. Hermann Hager. Mit zahlreichen in den Text gedruckten Holzschnitten. Achte Lieferung. (2. Band, 1. Lieferung.) Berlin 1883. Verlag von Jul. Springer. Preis 2 Mark.

Published in:

Archiv der Pharmazie, 1883, v. 221, n. 12, p. 969, doi. 10.1002/ardp.18832211244

By:

Hoffmann, G.

Publication type:

Article

Chemisch-technisches Repertorium. Uebersichtlich geordnete Mittheilungen der neuesten Erfindungen, Fortschritte und Verbesserungen auf dem Gebiete der technischen und industriellen Chemie mit Hinweis auf Maschinen, Apparate und Literatur. Herausgegeben von Dr. Emil Jacobsen. 1882. Zweites Halbjahr. Zweite Hälfte. Mit in den Text gedruckten Holzschnitten. Berlin, 1883. R. Gärtner's Verlagsbuchhandlung

Published in:

Archiv der Pharmazie, 1883, v. 221, n. 12, p. 969, doi. 10.1002/ardp.18832211243

By:

Hoffmann, G.

Publication type:

Article

Single-Walled Carbon Nanotube Networks: The Influence of Individual Tube-Tube Contacts on the Large-Scale Conductivity of Polymer Composites.

Published in:

Advanced Functional Materials, 2016, v. 26, n. 24, p. 4377, doi. 10.1002/adfm.201600435

By:

Bârsan, Oana A.;
Hoffmann, Günter G.;
van der Ven, Leendert G. J.;
de With, Gijsbertus

Publication type:

Article

Highly Selective SAM-Nanowire Hybrid NO2 Sensor: Insight into Charge Transfer Dynamics and Alignment of Frontier Molecular Orbitals.

Published in:

Advanced Functional Materials, 2014, v. 24, n. 5, p. 595, doi. 10.1002/adfm.201301478

By:

Hoffmann, Martin W. G.;
Prades, Joan Daniel;
Mayrhofer, Leonhard;
Hernandez‐Ramirez, Francisco;
Järvi, Tommi T.;
Moseler, Michael;
Waag, Andreas;
Shen, Hao

Publication type:

Article

Sensors: Highly Selective SAM-Nanowire Hybrid NO2 Sensor: Insight into Charge Transfer Dynamics and Alignment of Frontier Molecular Orbitals (Adv. Funct. Mater. 5/2014).

Published in:

Advanced Functional Materials, 2014, v. 24, n. 5, p. 566, doi. 10.1002/adfm.201470026

By:

Hoffmann, Martin W. G.;
Prades, Joan Daniel;
Mayrhofer, Leonhard;
Hernandez‐Ramirez, Francisco;
Järvi, Tommi T.;
Moseler, Michael;
Waag, Andreas;
Shen, Hao

Publication type:

Article

Spatial discrimination of glioblastoma and treatment effect with histologically-validated perfusion and diffusion magnetic resonance imaging metrics.

Published in:

Journal of Neuro-Oncology, 2018, v. 136, n. 1, p. 13, doi. 10.1007/s11060-017-2617-3

By:

Prah, Melissa A.;
Al-Gizawiy, Mona M.;
Mueller, Wade M.;
Cochran, Elizabeth J.;
Hoffmann, Raymond G.;
Connelly, Jennifer M.;
Schmainda, Kathleen M.

Publication type:

Article

Inborn errors of metabolism and motor disturbances in children.

Published in:

Journal of Inherited Metabolic Disease, 2009, v. 32, n. 5, p. 618, doi. 10.1007/s10545-009-1194-9

By:

García-Cazorla, A.;
Wolf, N.;
Serrano, M.;
Pérez-Dueñas, B.;
Pineda, M.;
Campistol, J.;
Fernández-Alvarez, E.;
Colomer, J.;
DiMauro, S.;
Hoffmann, G.

Publication type:

Article

Epilepsy and inborn errors of metabolism in children.

Published in:

Journal of Inherited Metabolic Disease, 2009, v. 32, n. 5, p. 609, doi. 10.1007/s10545-009-1171-3

By:

Wolf, N.;
García-Cazorla, A.;
Hoffmann, G.

Publication type:

Article

Mental retardation and inborn errors of metabolism.

Published in:

Journal of Inherited Metabolic Disease, 2009, v. 32, n. 5, p. 597, doi. 10.1007/s10545-009-0922-5

By:

García-Cazorla, A.;
Wolf, N.;
Serrano, M.;
Moog, U.;
Pérez-Dueñas, B.;
Póo, P.;
Pineda, M.;
Campistol, J.;
Hoffmann, G.

Publication type:

Article

Coenzyme Q10is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria.

Published in:

Journal of Inherited Metabolic Disease, 2009, v. 32, n. 4, p. 570, doi. 10.1007/s10545-009-1150-8

By:

Haas, D.;
Niklowitz, P.;
Hörster, F.;
Baumgartner, E. R.;
Prasad, C.;
Rodenburg, R. J.;
Hoffmann, G. F.;
Menke, T.;
Okun, J. G.

Publication type:

Article

Tetrahydrobiopterin deficiency in human rabies.

Published in:

Journal of Inherited Metabolic Disease, 2009, v. 32, n. 1, p. 65, doi. 10.1007/s10545-008-0949-z

By:

Willoughby, R.;
Opladen, T.;
Maier, T.;
Rhead, W.;
Schmiedel, S.;
Hoyer, J.;
Drosten, C.;
Rupprecht, C.;
Hyland, K.;
Hoffmann, G.

Publication type:

Article

Qualitative urinary organic acid analysis: Methodological approaches and performance.

Published in:

Journal of Inherited Metabolic Disease, 2008, v. 31, n. 6, p. 690, doi. 10.1007/s10545-008-0986-7

By:

Peters, V.;
Garbade, S.;
Langhans, C.;
Hoffmann, G.;
Pollitt, R.;
Downing, M.;
Bonham, J.

Publication type:

Article

Recurrent acute liver failure and mitochondriopathy in a case of Wolcott–Rallison syndrome.

Published in:

Journal of Inherited Metabolic Disease, 2008, v. 31, n. 4, p. 540, doi. 10.1007/s10545-008-0867-0

By:

Engelmann, G.;
Meyburg, J.;
Shahbek, N.;
Al-Ali, M.;
Hairetis, M.;
Baker, A.;
Rodenburg, R.;
Wenning, D.;
Flechtenmacher, C.;
Ellard, S.;
Smeitink, J.;
Hoffmann, G.;
Buchanan, C.

Publication type:

Article

Newborn screening for methylmalonic acidurias—Optimization by statistical parameter combination.

Published in:

Journal of Inherited Metabolic Disease, 2008, v. 31, n. 3, p. 379, doi. 10.1007/s10545-008-0892-z

By:

Lindner, M.;
Ho, S.;
Kölker, S.;
Abdoh, G.;
Hoffmann, G.;
Burgard, P.

Publication type:

Article

Liver cell transplantation for the treatment of inborn errors of metabolism.

Published in:

Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 164, doi. 10.1007/s10545-008-0829-6

By:

Meyburg, J.;
Hoffmann, G.

Publication type:

Article

Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism.

Published in:

Journal of Inherited Metabolic Disease, 2008, v. 31, n. 2, p. 194, doi. 10.1007/s10545-008-0823-z

By:

Kölker, S.;
Sauer, S.;
Hoffmann, G.;
Müller, I.;
Morath, M.;
Okun, J.

Publication type:

Article

Deletion of a single mevalonate kinase ( Mvk) allele yields a murine model of hyper-IgD syndrome.

Published in:

Journal of Inherited Metabolic Disease, 2007, v. 30, n. 6, p. 888, doi. 10.1007/s10545-007-0776-7

By:

Hager, E.;
Tse, H.;
Piganelli, J.;
Gupta, M.;
Baetscher, M.;
Tse, T.;
Pappu, A.;
Steiner, R.;
Hoffmann, G.;
Gibson, K.

Publication type:

Article

LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 gene.

Published in:

Journal of Inherited Metabolic Disease, 2007, v. 30, n. 4, p. 611, doi. 10.1007/s10545-007-0670-3

By:

Al-Dirbashi, O.;
Abu-Amero, K.;
Alswaid, A.;
Hoffmann, G.;
Al-Qahtani, K.;
Rashed, M.

Publication type:

Article

Focus on neonatal screening.

Published in:

2007

By:

Hoffmann, G.;
Pollitt, R.;
Torresani, T.;
Yamaguchi, S.

Publication type:

Editorial

Expanded newborn screening in Europe 2007.

Published in:

Journal of Inherited Metabolic Disease, 2007, v. 30, n. 4, p. 439, doi. 10.1007/s10545-007-0666-z

By:

Bodamer, O.;
Hoffmann, G.;
Lindner, M.

Publication type:

Article

Implementation of extended neonatal screening and a metabolic unit in the State of Qatar: Developing and optimizing strategies in cooperation with the Neonatal Screening Center in Heidelberg.

Published in:

Journal of Inherited Metabolic Disease, 2007, v. 30, n. 4, p. 522, doi. 10.1007/s10545-007-0553-7

By:

Lindner, M.;
Abdoh, G.;
Fang-Hoffmann, J.;
Shabeck, N.;
Sayrafi, M.;
Janahi, M.;
Ho, S.;
Abdelrahman, M.;
Ben-Omran, T.;
Bener, A.;
Schulze, A.;
Rifai, H.;
Thani, G.;
Hoffmann, G.

Publication type:

Article

Pyridoxal 5′-phosphate may be curative in early-onset epileptic encephalopathy.

Published in:

Journal of Inherited Metabolic Disease, 2007, v. 30, n. 1, p. 96, doi. 10.1007/s10545-006-0508-4

By:

Hoffmann, G.;
Schmitt, B.;
Windfuhr, M.;
Wagner, N.;
Strehl, H.;
Bagci, S.;
Franz, A.;
Mills, P.;
Clayton, P.;
Baumgartner, M.;
Steinmann, B.;
Bast, T.;
Wolf, N.;
Zschocke, J.

Publication type:

Article

Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).

Published in:

Journal of Inherited Metabolic Disease, 2007, v. 30, n. 1, p. 5, doi. 10.1007/s10545-006-0451-4

By:

Kölker, S.;
Christensen, E.;
Leonard, J.;
Greenberg, C.;
Burlina, A.;
Dixon, M.;
Duran, M.;
Goodman, S.;
Koeller, D.;
Müller, E.;
Naughten, E.;
Neumaier-Probst, E.;
Okun, J.;
Kyllerman, M.;
Surtees, R.;
Wilcken, B.;
Hoffmann, G.;
Burgard, P.

Publication type:

Article

Acrodermatitis acidaemia secondary to ‘overtreatment’ and protein deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2006, v. 29, n. 1, p. 173, doi. 10.1007/s10545-006-0345-5

By:

Hoffmann, G.;
Happle, R.;
Kölker, S.

Publication type:

Article

Comprehensive analysis of pyrimidine metabolism in 450 children with unspecific neurological symptoms using high–pressure liquid chromatography–electrospray ionization tandem mass spectrometry.

Published in:

Journal of Inherited Metabolic Disease, 2005, v. 28, n. 6, p. 1109, doi. 10.1007/s10545-005-0133-7

By:

Schmidt, C.;
Hofmann, U.;
Kohlmüller, D.;
Mürdter, T.;
Zanger, U.;
Schwab, M.;
Hoffmann, G.

Publication type:

Article

Fumarase deficiency presenting with periventricular cysts.

Published in:

2005

By:

Loeffen, J.;
Smeets, R.;
Voit, T.;
Hoffmann, G.;
Smeitink, J.

Publication type:

Report

Disorders of intermediary metabolism: Toxic leukoencephalopathies.

Published in:

Journal of Inherited Metabolic Disease, 2005, v. 28, n. 3, p. 345, doi. 10.1007/s10545-005-2164-5

By:

Hörster, F.;
Surtees, R.;
Hoffmann, G.

Publication type:

Article

Looking forward—An evidence-based approach to glutaryl-CoA dehydrogenase deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 921, doi. 10.1023/B:BOLI.0000045778.73581.7d

By:

KÖlker, S.;
Burgard, P.;
Okun, J.;
Schulze-Bergkamen, A.;
Assmann, B.;
Greenberg, C.;
Hoffmann, G.

Publication type:

Article

Management of movement disorders in glutaryl-CoA dehydrogenase deficiency: Anticholinergic drugs and botulinum toxin as additional therapeutic options.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 911, doi. 10.1023/B:BOLI.0000045776.50573.52

By:

Burlina, A.;
Zara, G.;
Hoffmann, G.;
Zschocke, J.

Publication type:

Article

Emergency treatment in glutaryl-CoA dehydrogenase deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 893, doi. 10.1023/B:BOLI.0000045774.51260.ea

By:

KÖlker, S.;
Greenberg, C.;
Lindner, M.;
Müller, E.;
Naughten, E.;
Hoffmann, G.

Publication type:

Article

Maintenance treatment of glutaryl-CoA dehydrogenase deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 885, doi. 10.1023/B:BOLI.0000045773.07785.83

By:

Mühlhausen, C.;
Hoffmann, G.;
Strauss, K.;
KÖlker, S.;
Okun, J.;
Greenberg, C.;
Naughten, E.;
Ullrich, K.

Publication type:

Article

Neonatal screening for glutaryl-CoA dehydrogenase deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 851, doi. 10.1023/B:BOLI.0000045769.96657.af

By:

Lindner, M.;
KÖlker, S.;
Schulze, A.;
Christensen, E.;
Greenberg, C.;
Hoffmann, G.

Publication type:

Article

Challenges for basic research in glutaryl-CoA dehydrogenase deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 843, doi. 10.1023/B:BOLI.0000045768.38073.22

By:

KÖlker, S.;
Strauss, K.;
Goodman, S.;
Hoffmann, G.;
Okun, J.;
Koeller, D.

Publication type:

Article

Modulation of glutamatergic and GABAergic neurotransmission in glutaryl-CoA dehydrogenase deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 825, doi. 10.1023/B:BOLI.0000045765.37043.fb

By:

Wajner, M.;
KÖlker, S.;
Souza, D.;
Hoffmann, G.;
de Mello, C.

Publication type:

Article

Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 805, doi. 10.1023/B:BOLI.0000045762.37248.28

By:

KÖlker, S.;
Koeller, D.;
Sauer, S.;
HÖrster, F.;
Schwab, M.;
Hoffmann, G.;
Ullrich, K.;
Okun, J.

Publication type:

Article

Improvement of CDG diagnosis by combined examination of several glycoproteins.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 5, p. 581, doi. 10.1023/B:BOLI.0000042982.82131.a4

By:

Fang, J.;
Peters, V.;
Körner, C.;
Hoffmann, G.

Publication type:

Article

Sedation with 4-hydroxybutyric acid: A potential pitfall in the diagnosis of SSADH deficiency.

Published in:

Journal of Inherited Metabolic Disease, 2004, v. 27, n. 2, p. 291, doi. 10.1023/B:BOLI.0000028842.15981.6e

By:

Wolf, N.;
Haas, D.;
Hoffmann, G.;
Jakobs, C.;
Salomons, G.;
Wevers, R.;
Engelke, U.;
Rating, D.

Publication type:

Article

Phenylalanine can be detected in brain tissue of healthy subjects by 1H magnetic resonance spectroscopy.

Published in:

Journal of Inherited Metabolic Disease, 2003, v. 26, n. 7, p. 683, doi. 10.1023/B:BOLI.0000005648.75276.71

By:

Pietz, J.;
Lutz, T.;
Zwygart, K.;
Hoffmann, G.;
Ebinger, F.;
Boesch, C.;
Kreis, R.

Publication type:

Article

Towards quality assurance in the determination of lysosomal enzymes: A two-centre study.

Published in:

Journal of Inherited Metabolic Disease, 2003, v. 26, n. 6, p. 571, doi. 10.1023/A:1025904132569

By:

Lukacs, Z.;
Keil, A.;
Peters, V.;
Kohlschütter, A.;
Hoffmann, G.;
Cantz, M.;
Kopitz, J.

Publication type:

Article

Emergency management of inherited metabolic diseases.

Published in:

Journal of Inherited Metabolic Disease, 2002, v. 25, n. 7, p. 531, doi. 10.1023/A:1022040422590

By:

Prietsch, V.;
Lindner, M.;
Zschocke, J.;
Nyhan, W.;
Hoffmann, G.

Publication type:

Article

Glutaric aciduria type III: A distinctive non-disease?

Published in:

Journal of Inherited Metabolic Disease, 2002, v. 25, n. 6, p. 483, doi. 10.1023/A:1021207419125

By:

Knerr, I.;
Zschocke, J.;
Trautmann, U.;
Dorland, L.;
de Koning, T.;
Müller, P.;
Christensen, E.;
Trefz, F.;
Wündisch, G.;
Rascher, W.;
Hoffmann, G.

Publication type:

Article

Neurotransmitter metabolites in CSF: An external quality control scheme.

Published in:

Journal of Inherited Metabolic Disease, 2002, v. 25, n. 4, p. 287, doi. 10.1023/A:1016550324235

By:

Bräutigam, C.;
Weykamp, C.;
Hoffmann, G.;
Wevers, R.

Publication type:

Article