Odenwald B - Search Results

1

Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples.

Maier EM, Mütze U, Janzen N, Steuerwald U, Nennstiel U, Odenwald B, Schuhmann E, Lotz-Havla AS, Weiss KJ, Hammersen J, Weigel C, Thimm E, Grünert SC, Hennermann JB, Freisinger P, Krämer J, Das AM, Illsinger S, Gramer G, Fang-Hoffmann J, Garbade SF, Okun JG, Hoffmann GF, Kölker S, Röschinger W. Maier EM, et al. Among authors: odenwald b. J Inherit Metab Dis. 2023 Nov;46(6):1043-1062. doi: 10.1002/jimd.12671. Epub 2023 Sep 12. J Inherit Metab Dis. 2023. PMID: 37603033

2

Newborn screening for carnitine transporter defect in Bavaria and the long-term follow-up of the identified newborns and mothers: Assessing the benefit and possible harm based on 19 ½ years of experience.

Schiergens KA, Weiss KJ, Röschinger W, Lotz-Havla AS, Schmitt J, Dalla Pozza R, Ulrich S, Odenwald B, Kreuder J, Maier EM. Schiergens KA, et al. Among authors: odenwald b. Mol Genet Metab Rep. 2021 Jun 12;28:100776. doi: 10.1016/j.ymgmr.2021.100776. eCollection 2021 Sep. Mol Genet Metab Rep. 2021. PMID: 34178604 Free PMC article.

3

Long-Term Course of Hypothyroidism Detected through Neonatal TSH Screening in a Population-Based Cohort of Very Preterm Infants Born at Less than 32 Weeks of Gestation.

Odenwald B, Fischer A, Röschinger W, Liebl B, Schmidt H, Nennstiel U. Odenwald B, et al. Int J Neonatal Screen. 2021 Oct 13;7(4):65. doi: 10.3390/ijns7040065. Int J Neonatal Screen. 2021. PMID: 34698071 Free PMC article.

4

Sudden neonatal death in individuals with medium-chain acyl-coenzyme A dehydrogenase deficiency: limit of newborn screening.

Mütze U, Nennstiel U, Odenwald B, Haase C, Ceglarek U, Janzen N, Garbade SF, Hoffmann GF, Kölker S, Haas D. Mütze U, et al. Among authors: odenwald b. Eur J Pediatr. 2022 Jun;181(6):2415-2422. doi: 10.1007/s00431-022-04421-y. Epub 2022 Mar 16. Eur J Pediatr. 2022. PMID: 35294644 Free PMC article.

5

Is Our Newborn Screening Working Well? A Literature Review of Quality Requirements for Newborn Blood Spot Screening (NBS) Infrastructure and Procedures.

Odenwald B, Brockow I, Hanauer M, Lüders A, Nennstiel U. Odenwald B, et al. Int J Neonatal Screen. 2023 Jun 22;9(3):35. doi: 10.3390/ijns9030035. Int J Neonatal Screen. 2023. PMID: 37489488 Free PMC article. Review.

6

[Newborn blood spot screening (NBS) in Germany : Status quo and presentation of a concept for further development].

Nennstiel U, Odenwald B, Throner V, Blankenstein O, Vieth A, Ratzel R, Coenen M, Brockow I. Nennstiel U, et al. Among authors: odenwald b. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2023 Nov;66(11):1195-1204. doi: 10.1007/s00103-023-03771-8. Epub 2023 Oct 10. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2023. PMID: 37815611 Free PMC article. Review. German.

7

Caring for a Child with Congenital Adrenal Hyperplasia Diagnosed by Newborn Screening: Parental Health-Related Quality of Life, Coping Patterns, and Needs.

Rautmann L, Witt S, Theiding C, Odenwald B, Nennstiel-Ratzel U, Dörr HG, Quitmann JH. Rautmann L, et al. Among authors: odenwald b. Int J Environ Res Public Health. 2023 Mar 3;20(5):4493. doi: 10.3390/ijerph20054493. Int J Environ Res Public Health. 2023. PMID: 36901502 Free PMC article.

8

Children with classic congenital adrenal hyperplasia experience salt loss and hypoglycemia: evaluation of adrenal crises during the first 6 years of life.

Odenwald B, Nennstiel-Ratzel U, Dörr HG, Schmidt H, Wildner M, Bonfig W. Odenwald B, et al. Eur J Endocrinol. 2016 Feb;174(2):177-86. doi: 10.1530/EJE-15-0775. Epub 2015 Nov 12. Eur J Endocrinol. 2016. PMID: 26563979

9

Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase-Deficiency: 13 Years of Neonatal Screening and Follow-up in Bavaria.

Odenwald B, Dörr HG, Bonfig W, Schmidt H, Fingerhut R, Wildner M, Nennstiel-Ratzel U. Odenwald B, et al. Klin Padiatr. 2015 Sep;227(5):278-83. doi: 10.1055/s-0035-1554639. Epub 2015 Jun 19. Klin Padiatr. 2015. PMID: 26090996

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