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Items: 1 to 20 of 35

1.

Continued high incidence of children with severe influenza A(H1N1)pdm09 admitted to paediatric intensive care units in Germany during the first three post-pandemic influenza seasons, 2010/11-2012/13.

Streng A, Prifert C, Weissbrich B, Liese JG; Bavarian PICU Study Group on Influenza and Other Viral ARI..

BMC Infect Dis. 2015 Dec 18;15:573. doi: 10.1186/s12879-015-1293-1.

2.

[Functional separation of the lungs. Ventilation strategy for unilateral blunt force thoracic trauma].

Hammersen G, Beiderlinden M.

Anaesthesist. 2012 Dec;61(12):1045-8. doi: 10.1007/s00101-012-2104-3. German.

PMID:
23223839
3.

Aortopulmonary window.

Koch AM, Hammersen G, Rüffer A.

Eur Heart J. 2012 May;33(10):1200. doi: 10.1093/eurheartj/ehr355. No abstract available.

PMID:
21937480
4.

Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey.

Raue F, Pichl J, Dörr HG, Schnabel D, Heidemann P, Hammersen G, Jaursch-Hancke C, Santen R, Schöfl C, Wabitsch M, Haag C, Schulze E, Frank-Raue K.

Clin Endocrinol (Oxf). 2011 Dec;75(6):760-5. doi: 10.1111/j.1365-2265.2011.04142.x.

PMID:
21645025
5.

Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.

Namavar Y, Barth PG, Kasher PR, van Ruissen F, Brockmann K, Bernert G, Writzl K, Ventura K, Cheng EY, Ferriero DM, Basel-Vanagaite L, Eggens VR, Krägeloh-Mann I, De Meirleir L, King M, Graham JM Jr, von Moers A, Knoers N, Sztriha L, Korinthenberg R; PCH Consortium., Dobyns WB, Baas F, Poll-The BT.

Brain. 2011 Jan;134(Pt 1):143-56. doi: 10.1093/brain/awq287.

PMID:
20952379
6.

Lethal cutis laxa with contractural arachnodactyly, overgrowth and soft tissue bleeding due to a novel homozygous fibulin-4 gene mutation.

Hoyer J, Kraus C, Hammersen G, Geppert JP, Rauch A.

Clin Genet. 2009 Sep;76(3):276-81. doi: 10.1111/j.1399-0004.2009.01204.x.

PMID:
19664000
7.

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia.

Budde BS, Namavar Y, Barth PG, Poll-The BT, Nürnberg G, Becker C, van Ruissen F, Weterman MA, Fluiter K, te Beek ET, Aronica E, van der Knaap MS, Höhne W, Toliat MR, Crow YJ, Steinling M, Voit T, Roelenso F, Brussel W, Brockmann K, Kyllerman M, Boltshauser E, Hammersen G, Willemsen M, Basel-Vanagaite L, Krägeloh-Mann I, de Vries LS, Sztriha L, Muntoni F, Ferrie CD, Battini R, Hennekam RC, Grillo E, Beemer FA, Stoets LM, Wollnik B, Nürnberg P, Baas F.

Nat Genet. 2008 Sep;40(9):1113-8. doi: 10.1038/ng.204.

PMID:
18711368
8.

Varicella-related deaths in children and adolescents--Germany 2003-2004.

Grote V, von Kries R, Springer W, Hammersen G, Kreth HW, Liese J.

Acta Paediatr. 2008 Feb;97(2):187-92.

PMID:
18076716
9.

Fetal adrenal haemorrhage--two-dimensional and three-dimensional imaging.

Schrauder MG, Hammersen G, Siemer J, Goecke TW, Meurer B, Hart N, Beckmann MW, Schild RL.

Fetal Diagn Ther. 2008;23(1):72-5.

PMID:
17934302
10.

Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation.

Pasutto F, Sticht H, Hammersen G, Gillessen-Kaesbach G, Fitzpatrick DR, Nürnberg G, Brasch F, Schirmer-Zimmermann H, Tolmie JL, Chitayat D, Houge G, Fernández-Martínez L, Keating S, Mortier G, Hennekam RC, von der Wense A, Slavotinek A, Meinecke P, Bitoun P, Becker C, Nürnberg P, Reis A, Rauch A.

Am J Hum Genet. 2007 Mar;80(3):550-60.

11.

A defect in dolichol phosphate biosynthesis causes a new inherited disorder with death in early infancy.

Kranz C, Jungeblut C, Denecke J, Erlekotte A, Sohlbach C, Debus V, Kehl HG, Harms E, Reith A, Reichel S, Grobe H, Hammersen G, Schwarzer U, Marquardt T.

Am J Hum Genet. 2007 Mar;80(3):433-40.

12.

CR3/108--Congenital alveolar capillary dysplasia with familiary microphthalmia.

Schirmer-Zimmerman H, Hammersen G, Scheuerlen W, Griese M, Brasch F, Rauch A.

Paediatr Respir Rev. 2006;7 Suppl 1:S326. No abstract available.

PMID:
17036407
13.
14.

The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients.

Gibson KM, Christensen E, Jakobs C, Fowler B, Clarke MA, Hammersen G, Raab K, Kobori J, Moosa A, Vollmer B, Rossier E, Iafolla AK, Matern D, Brouwer OF, Finkelstein J, Aksu F, Weber HP, Bakkeren JA, Gabreels FJ, Bluestone D, Barron TF, Beauvais P, Rabier D, Santos C, Lehnert W, et al.

Pediatrics. 1997 Apr;99(4):567-74.

PMID:
9093300
15.

[Echocardiographic diagnosis of congenital diverticuli of the right and left ventricle].

Wild F, Hofbeck M, Singer H, Hammersen G.

Klin Padiatr. 1993 May-Jun;205(3):167-9. German.

PMID:
8350590
16.

Intestinal amino acid absorption in the Fanconi syndrome: studies in patients and in rats with the maleic acid induced syndrome.

Nützenadel W, Fahr K, Hammersen G.

Pediatr Res. 1983 Sep;17(9):710-3. No abstract available.

PMID:
6622103
17.

Improved prenatal diagnosis of methylmalonic acidemia: mass fragmentography of methylmalonic acid in amniotic fluid and maternal urine.

Trefz FK, Schmidt H, Tauscher B, Depène E, Baumgartner R, Hammersen G, Kochen W.

Eur J Pediatr. 1981 Nov;137(3):261-6. No abstract available.

PMID:
7318836
18.

[Technique for intraventricular application of antibiotics in bacterial meningitis of the newborn (author's transl)].

Hammersen G, Wille L.

Monatsschr Kinderheilkd. 1981 Sep;129(9):525-8. German.

PMID:
7343830
19.

[Poisoning in children].

Hammersen G.

Med Monatsschr Pharm. 1980 Jun;3(6):161-7. German. No abstract available.

PMID:
7464671
20.

[Familial nesidioblastosis].

Trefz FK, Schmidt H, Hammersen G, Helmstädter V, Bolkenius M.

Monatsschr Kinderheilkd. 1980 May;128(5):337-8. German. No abstract available.

PMID:
6252458

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