heiBIB: Lindner, Martin

Lindner, Martin Dr.Universität HeidelbergHeidelberg

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englisch (32)
deutsch (5)

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Kulozik, Andreas (3)
Muckenthaler, Martina (3)
Happich, Margit (2)
Leichsenring, Michael (1954-2022) (2)
Bettendorf, Markus (2)
Schulze, Andreas (2)
Mall, Marcus A. (2)
Feneberg, Reinhard (2)
Okun, Jürgen G. (2)
Meyburg, Jochen (2)
Vill, Katharina (2)
Pfeil, Johannes (2)
Listl, Stefan (2)
Staufner, Christian (2)
Sommerburg, Olaf (2)
Autschbach, Frank (1)
Schirmacher, Peter (1)
Pöschl, Johannes (1)
Renner, Marcus (1)
Schnabel, Philipp Albert (1953-2021) (1)
Goeppert, Benjamin (1)
Tönshoff, Burkhard (1)
Haas, Dorothea (1)
Stahl, Mirjam (1)
Leible, Svenja (1)
Hörster, Friederike (1)
Ruef, Peter (1)
Völcker, Hans Eberhard (1)
Glahn, Esther M. (1)
Krastel, Hermann (1)
Kebbewar, Moustafa (1)
Gleich, Florian (1)
Förl, Birgit (1)
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Publikationen in heiBIB

Mütze, Ulrike: Long-term outcomes of individuals with metabolic diseases identified through newborn screening / Ulrike Mütze, MD, Sven F. Garbade, PhD, Gwendolyn Gramer, MD, Martin Lindner, MD, Peter Freisinger, … , October 13, 2020. - 11 S.
In: Pediatrics, ISSN 1098-4275. 146(2020,5) Artikelnummer e20200444, 11 Seiten
DOI: 10.1542/peds.2020-0444
Teufel-Schäfer, Ulrike: High blood pressure, a red flag for the neonatal manifestation of urea cycle disorders / Ulrike Teufel, Peter Burgard, Jochen Meyburg, Martin Lindner, Johannes Poeschl, Peter Ruef, Georg F.… . -
London: BioMed Central, 17 Jun. 2019. - 1 Online-Ressource (7 Seiten)
DOI: 10.1186/s13023-019-1055-z
Burgard, Peter: Diagnoseeröffnung : CME zertifizierte Fortbildung = / P. Burgard, M. Lindner, 2018. - 11 S.
In: Monatsschrift Kinderheilkunde, ISSN 1433-0474. 166(2018), 4, Seite 343-353
DOI: 10.1007/s00112-017-0390-1
Choukair, Daniela: Analysis of the functional muscle-bone unit of the forearm in patients with phenylketonuria by peripheral quantitative computed tomography / Daniela Choukair, Carolin Kneppo, Reinhard Feneberg, Eckhard Schönau, Martin Lindner, Stefan Kölker,… , 2017. - 8 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 40(2017), 2, Seite 219-226
DOI: 10.1007/s10545-016-0002-6
Gramer, Gwendolyn: Medium-chain Acyl-CoA dehydrogenase deficiency : evaluation of genotype-phenotype correlation in patients detected by newborn screening / Gwendolyn Gramer, Gisela Haege, Junmin Fang-Hoffmann, Georg F. Hoffmann, Claus R. Bartram, Katrin Hi… , 05 May 2015. - 12 S.
In: JIMD reports, ISSN 2192-8312. 23(2015), Seite 101-112
DOI: 10.1007/8904_2015_439
Opladen, Thomas: In vivo monitoring of urea cycle activity with 13C-acetate as a tracer of ureagenesis / Thomas Opladen, Martin Lindner, Anibh M. Das, Thorsten Marquardt, Aneal Khan, Sukru H. Emre, Barbara… , 2016. - 8 S.
In: Molecular genetics and metabolism, ISSN 1096-7206. 117(2016), 1, Seite 19-26
DOI: 10.1016/j.ymgme.2015.11.007
Kunz, Joachim: Significant prevalence of sickle cell disease in Southwest Germany : results from a birth cohort study indicate the necessity for newborn screening / Joachim B. Kunz, Saida Awad, Margit Happich, Lena Muckenthaler, Martin Lindner, Gwendolyn Gramer, Jü… , 2016. - 6 S.
In: Annals of hematology, ISSN 1432-0584. 95(2016), 3, Seite 397-402
DOI: 10.1007/s00277-015-2573-y
Staufner, Christian: Adenosine kinase deficiency : expanding the clinical spectrum and evaluating therapeutic options / Christian Staufner, Martin Lindner, Carlo Dionisi‐Vici, Peter Freisinger, Dries Dobbelaere, Claire D… , 2016. - 11 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 39(2016), 2, Seite 273-283
DOI: 10.1007/s10545-015-9904-y
Chien, Yin-Hsiu: Mudd’s disease (MAT I/III deficiency) : a survey of data for MAT1A homozygotes and compound heterozygotes / Yin-Hsiu Chien, Jose E. Abdenur, Federico Baronio, Allison Anne Bannick, Fernando Corrales, Maria Co…
In: Orphanet journal of rare diseases, ISSN 1750-1172. 10(2015) Artikel-Nummer 99, 21 Seiten
DOI: 10.1186/s13023-015-0321-y
Knauer-Fischer, Sabine: Clinical presentation and outcome in a series of 88 patients with the cblC defect / Sabine Fischer, Martina Huemer, Matthias Baumgartner, Federica Deodato, Diana Ballhausen, Avihu Bone… , 6 March 2014. - 10 S. : Diagramme
In: Journal of inherited metabolic disease, ISSN 1573-2665. 37(2014), 5, Seite 831-840
DOI: 10.1007/s10545-014-9687-6
Hoffmann, Georg F.: 50 years of newborn screening / Georg F. Hoffmann, Martin Lindner, J. Gerard Loeber, 14 February 2014. - 2 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 37(2014), 2, Seite 163-164
DOI: 10.1007/s10545-014-9688-5
Cornel, Martina C.: A framework to start the debate on neonatal screening policies in the EU : an Expert Opinion Document / Cornel, Martina C. ... Burgard, Peter; Hoffmann, Georg F.; Lindner, Martin ..., 2014. - 6 S.
In: European journal of human genetics, ISSN 1476-5438. 22(2014), 1, Seite 12-17
DOI: 10.1038/ejhg.2013.90
Rüegger, Corinne M.: Cross-sectional observational study of 208 patients with non-classical urea cycle disorders / Corinne M. Rüegger ; Martin Lindner ... Stefan Kölker ... Christian Staufner ... Peter Burgard .... - 10 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 37(2014), 1, S. 21-30
DOI: 10.1007/s10545-013-9624-0
Sommerburg, Olaf: Comparison of different IRT-PAP protocols to screen newborns for cystic fibrosis in three central European populations / Olaf Sommerburg ; Veronika Krulisova ; Jutta Hammermann ; Martin Lindner ; Mirjam Stahl ; Martina Mu… . - 9 S.
In: Journal of cystic fibrosis, ISSN 1873-5010. 13(2014), 1, S. 15-23
DOI: 10.1016/j.jcf.2013.06.003
Lindner, Martin: Defekte des Intermediärstoffwechsels : optimierte Strategien für das Neugeborenenscreening, Differential- und Konfirmationsdiagnostik, Behandlung und Langzeitergebnisse / vorgelegt von Martin Lindner, 2014. - Getr. Zählung : Ill., graph. Darst.
Pfeil, Johannes: Newborn screening by tandem mass spectrometry for glutaric aciduria type 1 : a cost-effectiveness analysis / Johannes Pfeil, Stefan Listl, Georg F. Hoffmann, Stefan Kölker, Martin Lindner and Peter Burgard, 17 October 2013. - 11 S.
In: Orphanet journal of rare diseases, ISSN 1750-1172. 8(2013), Artikel-ID 167, Seite 1-11
DOI: 10.1186/1750-1172-8-167
Gramer, Gwendolyn: Living with an inborn error of metabolism detected by newborn screening—Parents’ perspectives on child development and impact on family life / Gwendolyn Gramer, Gisela Haege, Esther M. Glahn, Georg F. Hoffmann, Martin Lindner, Peter Burgard, 2014. - 7 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 37(2014), 2, Seite 189-195
DOI: 10.1007/s10545-013-9639-6
Gramer, Gwendolyn: Visual functions in phenylketonuria : evaluating the dopamine and long-chain polyunsaturated fatty acids depletion hypotheses / Gwendolyn Gramer, Birgit Förl, Christina Springer, Petra Weimer, Gisela Haege, Friederike Mackensen,… , January 2013. - 7 S.
In: Molecular genetics and metabolism, ISSN 1096-7206. 108(2013), 1, Seite 1-7
DOI: 10.1016/j.ymgme.2012.10.021
Pfeil, Johannes: Newborn screening by tandem mass spectrometry for glutaric aciduria type 1 : a cost-effectiveness analysis / Johannes Pfeil, Stefan Listl, Georg F. Hoffmann, Stefan Kölker, Martin Lindner and Peter Burgard. -
London: BioMed Central, 2016. - 1 Online-Ressource (11 Seiten)
Kraus, Jan P.: Mutation analysis in 54 propionic acidemia patients / J.P. Kraus, E. Spector, S. Venezia, P. Estes, P.W. Chiang, G. Creadon-Swindell, S. Müllerleile, L. d… , January 2012. - 13 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 35(2012), 1, Seite 51-63
DOI: 10.1007/s10545-011-9399-0
Goeppert, Benjamin: Noncompaction myocardium in association with type Ib glycogen storage disease / Benjamin Goeppert, Martin Lindner, Monika Nadja Vogel, Arne Warth, Albrecht Stenzinger, Marcus Renne… , 31 July 2012. - 3 S.
In: Pathology, research and practice, ISSN 1618-0631. 208(2012), 10, Seite 620-622
DOI: 10.1016/j.prp.2012.06.007
Grünert, Sarah: Clinical and neurocognitive outcome in symptomatic isovaleric acidemia / Sarah C. Grünert, Udo Wendel, Martin Lindner, Michael Leichsenring, K. Otfried Schwab, Jerry Vockley…
In: Orphanet journal of rare diseases, ISSN 1750-1172. 7(2012) Artikelnummer 9, 9 Seiten
DOI: 10.1186/1750-1172-7-9
Burgard, Peter: Newborn screening programmes in Europe : arguments and efforts regarding harmonization : Part 2 - From screening laboratory results to treatment, follow-up and quality assurance / Peter Burgard, Kathrin Rupp, Martin Lindner, Gisela Haege, Tessel Rigter, Stephanie S. Weinreich, J.… . - 13 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 35(2012), 4, S. 613-625
DOI: 10.1007/s10545-012-9484-z
Häberle, Johannes: Suggested guidelines for the diagnosis and management of urea cycle disorders / Johannes Häberle, Nathalie Boddaert, Alberto Burlina, Anupam Chakrapani, Marjorie Dixon, Martina Hue… . -
London: BioMed Central, 2016. - 1 Online-Ressource (30 Seiten)
Nennstiel-Ratzel, Uta: Neugeborenenscreening auf Stoffwechsel- und Hormonstörungen : Herausforderungen in Klinik und Praxis / U. Nennstiel-Ratzel, G.F. Hoffmann, M. Lindner, 02 September 2011. - 7 S.
In: Monatsschrift Kinderheilkunde, ISSN 1433-0474. 159(2011), 9, Seite 814-820
DOI: 10.1007/s00112-011-2442-2
Lindner, Martin: Efficacy and outcome of expanded newborn screening for metabolic diseases : report of 10 years from South-West Germany / Martin Lindner, Gwendolyn Gramer, Gisela Haege, Junmin Fang-Hoffmann, Karl O. Schwab, Uta Tacke, Fri… , 2011. - 10 S.
In: Orphanet journal of rare diseases, ISSN 1750-1172. 6(2011), Artikel-ID 44, Seite 1-10
DOI: 10.1186/1750-1172-6-44
Grünert, Sarah: Propionic acidemia : neonatal versus selective metabolic screening / S. C. Grünert, S. Müllerleile, L. de Silva, M. Barth, M. Walter, K. Walter, T. Meissner, M. Lindner,… . - 9 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 35(2012), 1, S. 41-49
DOI: 10.1007/s10545-011-9419-0
Sommerburg, Olaf: Initial evaluation of a biochemical cystic fibrosis newborn screening by sequential analysis of immunoreactive trypsinogen and pancreatitis-associated protein (IRT/PAP) as a strategy that does not involve DNA testing in a Northern European population / Olaf Sommerburg, Martin Lindner, Martina Muckenthaler, Dirk Kohlmueller, Svenja Leible, Reinhard Fen… , 17 August 2010. - 9 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 33(2010), Suppl 2, Seite S263-271
DOI: 10.1007/s10545-010-9174-7
Gan-Schreier, Hongying: Newborn population screening for classic homocystinuria by determination of total homocysteine from guthrie cards / Hongying Gan-Schreier, PhD, Moustafa Kebbewar, Junmin Fang-Hoffmann, MD, Julia Wilrich, MD, Ghassan … , March 2010. - 6 S.
In: The journal of pediatrics, ISSN 1097-6833. 156(2010), 3 vom: März, Seite 427-432
DOI: 10.1016/j.jpeds.2009.09.054
Popek, Manuela: Two inborn errors of metabolism in a newborn : glutaric aciduria type I combined with isobutyrylglycinuria / Manuela Popek, Melanie Walter, Malkanthi Fernando, Martin Lindner, Karl Otfried Schwab, Jörn Oliver … , 15 September 2010. - 5 S.
In: Clinica chimica acta, ISSN 1873-3492. 411(2010), 23 vom: Sept., Seite 2087-2091
DOI: 10.1016/j.cca.2010.09.006
Lindner, Martin: Newborn screening for disorders of fatty-acid oxidation : experience and recommendations from an expert meeting / Martin Lindner, Georg F. Hoffmann, Dietrich Matern, 7 April 2010. - 6 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 33(2010), 5 vom: Okt., Seite 521-526
DOI: 10.1007/s10545-010-9076-8
Wendel, Udo: Neugeborenen-Screening in Deutschland : positiver Screeningbefund - was ist zu tun? / Udo Wendel; Martin Lindner; Markus Bettendorf. - 1. Aufl (Online-Ausg.). -
Stuttgart: Schattauer Verlag, 2008. - Online-Ressource (104 S.), ISBN 978-3-7945-8095-8
Wendel, Udo: Neugeborenen-Screening in Deutschland : positiver Screeningbefund - was ist zu tun? / Udo Wendel; Martin Lindner; Markus Bettendorf. - 1. Aufl.. -
Stuttgart [u.a.]: Schattauer, 2009. - XI, 93 S., ISBN 978-3-7945-2686-4
Schulze, Andreas: Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry : results, outcome, and implications / Andreas Schulze, Martin Lindner, Dirk Kohlmüller, Katharina Olgemöller, Ertan Mayatepek, Georg F. Ho… , June 1, 2003. - 8 S.
In: Pediatrics, ISSN 1098-4275. 111(2003), 6, Seite 1399-1406
DOI: 10.1542/peds.111.6.1399
Okun, Jürgen G.: A method for quantitative acylcarnitine profiling in human skin fibroblasts using unlabelled palmitic acid : diagnosis of fatty acid oxidation disorders and differentiation between biochemical phenotypes of MCAD deficiency / Jürgen G Okun, Stefan Kölker, Andreas Schulze, Dirk Kohlmüller, Katharina Olgemöller, Martin Lindner… , 19 September 2002. - 8 S.
In: Biochimica et biophysica acta, ISSN 1879-2618. 1584(2002), 2, Seite 91-98
DOI: 10.1016/S1388-1981(02)00296-2

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