Publikationsliste Dr. Kerstin Walter

Erschienen in: Verschiedenes
Bücher
1. Huppelsberg, Walter: „Physiologie“ Kurzlehrbuch, Georg Thieme Verlag 2003, 2005, 2009 ISBN-10: 3131364327

2. Walter: „Fallbuch Physiologie“, Georg Thieme Verlag 2005, ISBN-10: 3131404310

3. Thieme (Hrsg.) Prüfungswissen Physikum 2009, ISBN: 9783131452214

4. Schwarze Reihe 2. ÄP 2006, 2007, 2008, 2009, 2010, 2011 (Kommentare Gynäkolo-gie/Geburtshilfe und Pädiatrie) Georg Thieme Verlag, ISBN: 9783131488725

Fachartikel
1. Grünert SC, Müllerleile S, De Silva L, Barth M, Walter M, Walter K, Meissner T, Lindner M, Ensenauer R, Santer R, Bodamer OA, Baumgartner MR, Brunner-Krainz M, Karall D, Haase C, Knerr I, Marquardt T, Hennermann JB, Steinfeld R, Beblo S, Koch HG, Konstantopoulou V, Scholl-Bürgi S, Van Teeffelen-Heithoff A, Suormala T, Sperl W, Kraus JP, Superti-Furga A, Schwab KO, Sass JO. Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients. Orphanet J Rare Dis. 2013 Jan 10;8(1):6.

2. Walter KN, Montgomery J, Amess P, Rabe H. Hyponatraemia and Brain Oedema in Newborns Following Oral Water Intoxication during Prolonged Labour. Klin Padiatr. 2012 Jul;224(4):266-267. Epub 2012 Mar 22.

3. Mahoney L, Crook D, Walter KN, Sherman E, Rabe H. What ist he Evidence for the use of Adrenaline in the Treatment of Neonatal Hypotension? Cardiovasc Hematol Agents Med Chem. 2012 Mar 1; 10(1):50-98

4. Kraus JP, Spector E, Venezia S, Estes P, Chiang PW, Creadon-Swindell G, Müllerleile S, de Sil-va L, Barth M, Walter M, Walter K, Meissner T, Lindner M, Ensenauer R, Santer R, Bodamer OA, Baumgartner MR, Brunner-Krainz M, Karall D, Haase C, Knerr I, Marquardt T, Hennermann JB, Steinfeld R, Beblo S, Koch HG, Konstantopoulou V, Scholl-Bürgi S, van Teeffelen-Heithoff A, Suormala T, Ugarte M, Sperl W, Superti-Furga A, Schwab KO, Grünert SC, Sass JO. Mutation analysis in 54 propionic acidemia patients. J Inherit Metab Dis. 2011 Oct 27.

5. Grünert SC, Müllerleile S, de Silva L, Barth M, Walter M, Walter K, Meissner T, Lindner M, Ensenauer R, Santer R, Bodamer OA, Baumgartner MR, Brunner-Krainz M, Karall D, Haase C, Knerr I, Marquardt T, Hennermann JB, Steinfeld R, Beblo S, Koch HG, Konstantopoulou V, Scholl-Bürgi S, van Teeffelen-Heithoff A, Suormala T, Sperl W, Kraus JP, Superti-Furga A, Schwab KO, Sass JO. Propionic acidemia: neonatal versus selective metabolic screening. J Inherit Metab Dis. 2011 Dec 2.

6. Walter KN, Heike R. Genital oedema associated with femoral central venous access in a premature baby. BMJ Case Reports, 2010;10

7. Walter KN, Bross F, Omran H. Großer kongenitaler Nävus mit Melanin-Ablagerungen im ZNS. Monatsschrift Kinderheilkunde Volume 158, Number 5, 480-482

8. Walter KN, Kienzle FB, Frankenschmidt A, Hiort O, Wudy SA, van der Werf-Grohmann N, Super-ti-Furga A, Schwab KO. Difficulties in Diagnosis and Treatment of 5a-reductase type 2-deficiency in a newborn with 46,XY DSD. Horm Res Paediatr. 2010 Jul;74(1):67-71. Epub 2010 Apr 16.
9. Walter KN, Erlacher M, Uhl M, Budde U, Nowak G, Superti-Furga A, Zieger B. Lepirudin treat-ment in a girl with iliac vein thrombosis, severe pulmonary embolism and suspected hep-arin-induced thrombocytopenia (HIT) II. Klin Padiatr. 2009 May-Jun;221(3):174-5.

10. Cybulla M, Walter KN, Schwarting A, Divito R, Feriozzi S, Sunder-Plassmann G; on behalf of the European FOS Investigators Group. Kidney transplantation in patients with Fabry disease. Transpl Int. 2009 Apr;22(4):475-81

11. Walter KN, Kratz C, Uhl M, Niemeyer C. Chemotherapy as a therapeutic option for congenital neuroblastoma complicated by paraplegia. Klin Padiatr. 2008 May-Jun;220(3):175-7.

12. Geiger J, Walter K, Uhl M, Bley TA, Jüttner E, Brink I, Kirschbaum A, Langer M, Kontny U. Imag-ing findings in a 3-year-old girl with type III pleuropulmonary blastoma. In Vivo. 2007 Nov-Dec;21(6):1119-22.

13. Cybulla M, Walter K, Neumann HP, Widmer U, Scharer M, Sunder-Plassmann G, Jansen T, Rolfs A, Beck M. Fabry disease: demographic data since introduction of enzyme replacement therapy Dtsch Med Wochenschr. 2007 Jul 5;132(28-29):1505-9. German.

14. Walter K, Tansek M, Tobias ES, Ikegawa S, Coucke P, Hyland J, Mortier G, Iwaya T, Nishimura G, Superti-Furga A, Unger S. COL2A1-related skeletal dysplasias with predominant metaph-yseal involvement. Am J Med Genet A. 2007 Jan 15;143(2):161-7.

15. Cybulla M, Kleber M, Walter KN, Kroeber SM, Neumann HP, Engelhardt M. Is Fabry disease associated with leukaemia? Br J Haematol. 2006 Oct;135(2):264-5. Epub 2006 Aug 31.

16. Walter KN, Greenhalgh KL, Newbury-Ecob RA, Kohlhase J. Mosaic trisomy 8 and Townes-Brocks syndrome due to a novel SALL1 mutation in the same patient. Am J Med Genet A. 2006 Mar 15;140(6):649-51.
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