Fang-Hoffmann, JunminUniversität HeidelbergHeidelberg
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Co-Autoren (Uni Heidelberg)
- Burgard, Peter (3)
- Feyh, Patrik (3)
- Peters, Verena (3)
- Haas, Dorothea (2)
- Haege, Gisela (2)
- Posset, Roland (2)
- Hörster, Friederike (2)
- Gleich, Florian (2)
- Assmann, Birgit (2)
- Klinke, Glynis (2)
- Monostori, Péter (2)
- Walter, Magdalena (2)
- Sauer, Sven (1)
- Morath, Marina (1)
- Leichsenring, Michael (1954-2022) (1)
- Kebbewar, Moustafa (1)
- Ediga, Raga (1)
- Hinderhofer, Katrin (1)
- Schnabel-Besson, Elena (1)
- Prietsch, Viola (1)
- Keller, Mareike (1)
- Weiss, Karl Heinz (1)
- Wilrich, Julia (1)
- Gan-Schreier, Hongying (1)
- Zschocke, Johannes (1)
- Grohmann-Held, Karina (1)
- Syrbe, Steffen (1)
- Boy, Nikolas (1)
- Bartram, Claus R. (1)
- Staufner, Christian (1)
- Sommerburg, Olaf (1)
Co-Autoren (extern)
- Brockow, Inken (1)
- Bener, Abdulbari (1)
- Illsinger, Sabine (1)
- Krämer, Johannes (1)
- Maier, Esther M. (1)
- Mengel, Eugen (1)
- Trefz, Friedrich K. (1)
- Schwab, Karl O. (1)
- Labitzke, Christiane (1)
- Ben-Omran, Tawfeg (1)
- Leichsenring, Michael (1)
- Reiter, G. (1)
- Penzien, J. M. (1)
- Körner, C. (1)
- Heidemann, P. H. (1)
- Jakobi, R. (1)
- Helwig-Rolig, Angelika (1)
- Tacke, Uta (1)
- Röschinger, Wulf (1)
- Shahbek, Noora (1)
- Al Rifai, Hilal (1)
- Al Khal, Abdul Latif (1)
- Wendel, Udo (1)
Neueste Publikationen in heiBIB 
(ingesamt sind 15 Publikationen erfasst)
- Maier, Esther M.: Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples / Esther M. Maier, Ulrike Mütze, Nils Janzen, Ulrike Steuerwald, Uta Nennstiel, Birgit Odenwald, Elfri… , 2023. - 20 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. (2023), Seite 1-20
DOI: 10.1002/jimd.12671
- Schnabel-Besson, Elena: Combined newborn screening allows comprehensive identification also of attenuated phenotypes for methylmalonic acidurias and homocystinuria / Elena Schnabel, Stefan Kölker, Florian Gleich, Patrik Feyh, Friederike Hörster, Dorothea Haas, Junmi… , 2023. - 15 S. : Illustrationen
In: Nutrients, ISSN 2072-6643. 15(2023), 15, Artikel-ID 3355, Seite 1-15
DOI: 10.3390/nu15153355
- Gramer, Gwendolyn: Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis : implications for process quality and patient care / Gwendolyn Gramer, Inken Brockow, Christiane Labitzke, Junmin Fang-Hoffmann, Andreas Beivers, Patrik … , 2021. - 11 S.
In: European journal of pediatrics, ISSN 1432-1076. 180(2021), 4, Seite 1145-1155
DOI: 10.1007/s00431-020-03849-4
- Mütze, Ulrike: Health outcomes of infants with vitamin B12 deficiency identified by newborn screening and early treated / Ulrike Mütze, MD, Magdalena Walter, PhD, Mareike Keller, MSc, Gwendolyn Gramer, MD, Sven F. Garbade,… , 11 February 2021. - 7 S.
In: The journal of pediatrics, ISSN 1097-6833. 235(2021) vom: Aug., Seite 42-48
DOI: 10.1016/j.jpeds.2021.02.009
- 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
- Gramer, Gwendolyn: Newborn screening for vitamin B12 deficiency in Germany : strategies, results, and public health implications / Gwendolyn Gramer, MD, Junmin Fang-Hoffmann, MD, Patrik Feyh, Glynis Klinke, PhD, Peter Monostori, Ph… , 2020. - 12 S.
In: The journal of pediatrics, ISSN 1097-6833. 216(2020) Artikel-Nummer 165-172.e4, 12 Seiten
DOI: 10.1016/j.jpeds.2019.07.052
- Gramer, Gwendolyn: High incidence of maternal vitamin B12 deficiency detected by newborn screening : first results from a study for the evaluation of 26 additional target disorders for the German newborn screening panel / Gwendolyn Gramer, Junmin Fang-Hoffmann, Patrik Feyh, Glynis Klinke, Peter Monostori, Jürgen G. Okun,… , 15 June 2018. - 12 S.
In: World journal of pediatrics, ISSN 1867-0687. 14(2018), 5, Seite 470-481
DOI: 10.1007/s12519-018-0159-1
- Gramer, Gwendolyn: Newborn screening for remethylation disorders and vitamin B<Subscript>12</Subscript> deficiency-evaluation of new strategies in cohorts from Qatar and Germany / Gwendolyn Gramer, Ghassan Abdoh, Tawfeg Ben-Omran, Noora Shahbeck, Rehab Ali, Laila Mahmoud, Junmin … . - 8 S.
In: World journal of pediatrics, ISSN 1867-0687. 13(2017), 2, S. 136-143
DOI: 10.1007/s12519-017-0003-z
- Staufner, Christian: Genetic cause and prevalence of hydroxyprolinemia / Christian Staufner, Tobias B. Haack, Patrik Feyh, Gwendolyn Gramer, Deepthi Ediga Raga, Caterina Ter… , 2 May 2016. - 8 S.
In: Journal of inherited metabolic disease, ISSN 1573-2665. 39(2016), 5, Seite 625-632
DOI: 10.1007/s10545-016-9940-2
- 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
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