Oheim R - Search Results

1

Autosomal recessive hypophosphatemic rickets type 2 (ARHR2) due to ENPP1-deficiency.

Höppner J, Kornak U, Sinningen K, Rutsch F, Oheim R, Grasemann C. Höppner J, et al. Among authors: oheim r. Bone. 2021 Dec;153:116111. doi: 10.1016/j.bone.2021.116111. Epub 2021 Jul 9. Bone. 2021. PMID: 34252603 Free article. Review.

2

A Novel ANO5 Mutation Causing Gnathodiaphyseal Dysplasia With High Bone Turnover Osteosclerosis.

Rolvien T, Koehne T, Kornak U, Lehmann W, Amling M, Schinke T, Oheim R. Rolvien T, et al. Among authors: oheim r. J Bone Miner Res. 2017 Feb;32(2):277-284. doi: 10.1002/jbmr.2980. Epub 2016 Sep 9. J Bone Miner Res. 2017. PMID: 27541832 Free article.

3

A novel COL1A2 C-propeptide cleavage site mutation causing high bone mass osteogenesis imperfecta with a regional distribution pattern.

Rolvien T, Kornak U, Stürznickel J, Schinke T, Amling M, Mundlos S, Oheim R. Rolvien T, et al. Among authors: oheim r. Osteoporos Int. 2018 Jan;29(1):243-246. doi: 10.1007/s00198-017-4224-8. Epub 2017 Sep 15. Osteoporos Int. 2018. PMID: 28916840

4

Clinical Significance of DXA and HR-pQCT in Autosomal Dominant Osteopetrosis (ADO II).

Butscheidt S, Rolvien T, Kornak U, Schmidt FN, Schinke T, Amling M, Oheim R. Butscheidt S, et al. Among authors: oheim r. Calcif Tissue Int. 2018 Jan;102(1):41-52. doi: 10.1007/s00223-017-0332-x. Epub 2017 Oct 10. Calcif Tissue Int. 2018. PMID: 29018903

5

Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2.

Butscheidt S, Delsmann A, Rolvien T, Barvencik F, Al-Bughaili M, Mundlos S, Schinke T, Amling M, Kornak U, Oheim R. Butscheidt S, et al. Among authors: oheim r. Osteoporos Int. 2018 Jul;29(7):1643-1651. doi: 10.1007/s00198-018-4499-4. Epub 2018 Mar 29. Osteoporos Int. 2018. PMID: 29594386

6

Comparison of Bone Microarchitecture Between Adult Osteogenesis Imperfecta and Early-Onset Osteoporosis.

Rolvien T, Stürznickel J, Schmidt FN, Butscheidt S, Schmidt T, Busse B, Mundlos S, Schinke T, Kornak U, Amling M, Oheim R. Rolvien T, et al. Among authors: oheim r. Calcif Tissue Int. 2018 Nov;103(5):512-521. doi: 10.1007/s00223-018-0447-8. Epub 2018 Jun 26. Calcif Tissue Int. 2018. PMID: 29946973

7

A novel FAM20C mutation causing hypophosphatemic osteomalacia with osteosclerosis (mild Raine syndrome) in an elderly man with spontaneous osteonecrosis of the knee.

Rolvien T, Kornak U, Schinke T, Amling M, Oheim R. Rolvien T, et al. Among authors: oheim r. Osteoporos Int. 2019 Mar;30(3):685-689. doi: 10.1007/s00198-018-4667-6. Epub 2018 Aug 27. Osteoporos Int. 2019. PMID: 30151622

8

Wnt1 is an Lrp5-independent bone-anabolic Wnt ligand.

Luther J, Yorgan TA, Rolvien T, Ulsamer L, Koehne T, Liao N, Keller D, Vollersen N, Teufel S, Neven M, Peters S, Schweizer M, Trumpp A, Rosigkeit S, Bockamp E, Mundlos S, Kornak U, Oheim R, Amling M, Schinke T, David JP. Luther J, et al. Among authors: oheim r. Sci Transl Med. 2018 Nov 7;10(466):eaau7137. doi: 10.1126/scitranslmed.aau7137. Sci Transl Med. 2018. PMID: 30404864

9

Mice lacking plastin-3 display a specific defect of cortical bone acquisition.

Yorgan TA, Sari H, Rolvien T, Windhorst S, Failla AV, Kornak U, Oheim R, Amling M, Schinke T. Yorgan TA, et al. Among authors: oheim r. Bone. 2020 Jan;130:115062. doi: 10.1016/j.bone.2019.115062. Epub 2019 Oct 31. Bone. 2020. PMID: 31678489 Free article.

10

Human Heterozygous ENPP1 Deficiency Is Associated With Early Onset Osteoporosis, a Phenotype Recapitulated in a Mouse Model of Enpp1 Deficiency.

Oheim R, Zimmerman K, Maulding ND, Stürznickel J, von Kroge S, Kavanagh D, Stabach PR, Kornak U, Tommasini SM, Horowitz MC, Amling M, Thompson D, Schinke T, Busse B, Carpenter TO, Braddock DT. Oheim R, et al. J Bone Miner Res. 2020 Mar;35(3):528-539. doi: 10.1002/jbmr.3911. Epub 2019 Dec 5. J Bone Miner Res. 2020. PMID: 31805212 Free PMC article.

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