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Items: 1 to 20 of 182


Outcomes of Mini-Open Carpal Tunnel Release in Patients With Unrecordable Preoperative Nerve Conduction Potentials at a Minimum of 5 Years.

Zhang D, Ostergaard P, Cefalu C, Hall M, Earp BE, Blazar P.

Hand (N Y). 2019 Jun 22:1558944719857815. doi: 10.1177/1558944719857815. [Epub ahead of print]


Clinical and molecular characterization of familial exudative vitreoretinopathy associated with microcephaly.

Hull S, Arno G, Ostergaard P, Pontikos N, Robson AG, Webster AR, Hogg CR, Wright GA, Henderson RHH, Martin CA, Jackson AP, Mansour S, Moore AT, Michaelides M.

Am J Ophthalmol. 2019 May 8. pii: S0002-9394(19)30193-X. doi: 10.1016/j.ajo.2019.05.001. [Epub ahead of print]


Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Fotiou E, Martin-Almedina S, Simpson MA, Lin S, Gordon K, Brice G, Atton G, Jeffery I, Rees DC, Mignot C, Vogt J, Homfray T, Snyder MP, Rockson SG, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.

Nat Commun. 2019 Apr 26;10(1):1951. doi: 10.1038/s41467-019-09905-4.


A Novel Mutation of KIF11 in a Child with 22q11.2 Deletion Syndrome Associated with MCLMR.

Güneş N, Taşdemir E, Jeffery H, Yetik H, Ostergaard P, Tüysüz B.

Mol Syndromol. 2019 Jan;9(5):266-270. doi: 10.1159/000491568. Epub 2018 Jul 20.


Considerations in the Treatment of Osteoporotic Distal Radius Fractures in Elderly Patients.

Ostergaard PJ, Hall MJ, Rozental TD.

Curr Rev Musculoskelet Med. 2019 Mar;12(1):50-56. doi: 10.1007/s12178-019-09531-z. Review.


The QTc interval and risk of cardiac events in bulimia nervosa: A long-term follow-up study.

Frederiksen TC, Christiansen MK, Østergaard PC, Thomsen PH, Graff C, Clausen L, Jensen HK.

Int J Eat Disord. 2018 Dec;51(12):1331-1338. doi: 10.1002/eat.22984. Epub 2018 Dec 6.


A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon.

Nadarajah N, Schulte D, McConnell V, Martin-Almedina S, Karapouliou C, Mortimer PS, Jeffery S, Schulte-Merker S, Gordon K, Mansour S, Ostergaard P.

Int J Mol Sci. 2018 Aug 1;19(8). pii: E2259. doi: 10.3390/ijms19082259.


Matrix stiffness controls lymphatic vessel formation through regulation of a GATA2-dependent transcriptional program.

Frye M, Taddei A, Dierkes C, Martinez-Corral I, Fielden M, Ortsäter H, Kazenwadel J, Calado DP, Ostergaard P, Salminen M, He L, Harvey NL, Kiefer F, Mäkinen T.

Nat Commun. 2018 Apr 17;9(1):1511. doi: 10.1038/s41467-018-03959-6.


Human phenotypes caused by PIEZO1 mutations; one gene, two overlapping phenotypes?

Martin-Almedina S, Mansour S, Ostergaard P.

J Physiol. 2018 Mar 15;596(6):985-992. doi: 10.1113/JP275718. Epub 2018 Jan 31. Review.


Enrichment of megabase-sized DNA molecules for single-molecule optical mapping and next-generation sequencing.

Łopacińska-Jørgensen JM, Pedersen JN, Bak M, Mehrjouy MM, Sørensen KT, Østergaard PF, Bilenberg B, Kristensen A, Taboryski RJ, Flyvbjerg H, Marie R, Tommerup N, Silahtaroglu A.

Sci Rep. 2017 Dec 20;7(1):17893. doi: 10.1038/s41598-017-18091-6.


VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations.

Hägerling R, Drees D, Scherzinger A, Dierkes C, Martin-Almedina S, Butz S, Gordon K, Schäfers M, Hinrichs K, Ostergaard P, Vestweber D, Goerge T, Mansour S, Jiang X, Mortimer PS, Kiefer F.

JCI Insight. 2017 Aug 17;2(16). pii: 93424. doi: 10.1172/jci.insight.93424. eCollection 2017 Aug 17.


Human venous valve disease caused by mutations in FOXC2 and GJC2.

Lyons O, Saha P, Seet C, Kuchta A, Arnold A, Grover S, Rashbrook V, Sabine A, Vizcay-Barrena G, Patel A, Ludwinski F, Padayachee S, Kume T, Kwak BR, Brice G, Mansour S, Ostergaard P, Mortimer P, Jeffery S, Brown N, Makinen T, Petrova TV, Modarai B, Smith A.

J Exp Med. 2017 Jul 19. pii: jem.20160875. doi: 10.1084/jem.20160875. [Epub ahead of print]


Oral health-related quality of life in socially endangered persons in Copenhagen, Denmark.

Øzhayat EB, Østergaard P, Gotfredsen K.

Acta Odontol Scand. 2016 Nov;74(8):620-625. doi: 10.1080/00016357.2016.1229022. Epub 2016 Sep 7.


EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.

Martin-Almedina S, Martinez-Corral I, Holdhus R, Vicente A, Fotiou E, Lin S, Petersen K, Simpson MA, Hoischen A, Gilissen C, Jeffery H, Atton G, Karapouliou C, Brice G, Gordon K, Wiseman JW, Wedin M, Rockson SG, Jeffery S, Mortimer PS, Snyder MP, Berland S, Mansour S, Makinen T, Ostergaard P.

J Clin Invest. 2016 Aug 1;126(8):3080-8. doi: 10.1172/JCI85794. Epub 2016 Jul 11.


The type and prevalence of the use of analgesics among inpatients in a geriatric psychiatry department.

Østergaard PJ, Gustafsson LN, Høyer EH, Munk-Jørgensen P.

Ther Adv Psychopharmacol. 2016 Feb;6(1):13-21. doi: 10.1177/2045125315619557.


Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Fotiou E, Martin-Almedina S, Simpson MA, Lin S, Gordon K, Brice G, Atton G, Jeffery I, Rees DC, Mignot C, Vogt J, Homfray T, Snyder MP, Rockson SG, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.

Nat Commun. 2015 Sep 3;6:8085. doi: 10.1038/ncomms9085. Erratum in: Nat Commun. 2019 Apr 26;10(1):1951.


The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome.

Joyce S, Gordon K, Brice G, Ostergaard P, Nagaraja R, Short J, Moore S, Mortimer P, Mansour S.

Eur J Hum Genet. 2016 May;24(5):690-6. doi: 10.1038/ejhg.2015.175. Epub 2015 Aug 5.


Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11.

Balikova I, Robson AG, Holder GE, Ostergaard P, Mansour S, Moore AT.

Acta Ophthalmol. 2016 Feb;94(1):92-8. doi: 10.1111/aos.12759. Epub 2015 May 21.


Mutations in TUBGCP4 alter microtubule organization via the γ-tubulin ring complex in autosomal-recessive microcephaly with chorioretinopathy.

Scheidecker S, Etard C, Haren L, Stoetzel C, Hull S, Arno G, Plagnol V, Drunat S, Passemard S, Toutain A, Obringer C, Koob M, Geoffroy V, Marion V, Strähle U, Ostergaard P, Verloes A, Merdes A, Moore AT, Dollfus H.

Am J Hum Genet. 2015 Apr 2;96(4):666-74. doi: 10.1016/j.ajhg.2015.02.011. Epub 2015 Mar 26.


The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review.

Atton G, Gordon K, Brice G, Keeley V, Riches K, Ostergaard P, Mortimer P, Mansour S.

Eur J Hum Genet. 2015 Dec;23(12):1634-9. doi: 10.1038/ejhg.2015.41. Epub 2015 Mar 25. Review.

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