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1

Using ImageJ for the quantitative analysis of flow-based adhesion assays in real-time under physiologic flow conditions

Meyer dos Santos, Sascha, Klinkhardt, Ute, Schneppenheim, Reinhard, Harder, Sebastian

Journal:

Year:

2010

Language:

english

File:

PDF, 1.16 MB

english, 2010

2

Characterization of VWF gene conversions causing von Willebrand disease

Ahmad, Firdos, Kannan, Meganathan, Obser, Tobias, Budde, Ulrich, Schneppenheim, Sonja, Saxena, Renu, Schneppenheim, Reinhard

Journal:

British Journal of Haematology

Year:

2018

Language:

english

File:

PDF, 336 KB

english, 2018

3

The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: Key findings at enrolment until 2017

van Dorland, Hendrika A., Mansouri Taleghani, Magnus, Sakai, Kazuya, Friedman, Kenneth D, George, James N, Hrachovinova, Ingrid, Knöbl, Paul N, von Krogh, Anne Sophie, Schneppenheim, Reinhard, Aebi-Hu

Journal:

Year:

2019

Language:

english

File:

PDF, 1.94 MB

english, 2019

4

Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor

Uwe Kordes, Stefan Gesk, Michael Christoph Frühwald, Norbert Graf, Ivo Leuschner, Martin Hasselblatt, Astrid Jeibmann, Florian Oyen, Ove Peters, Torsten Pietsch, Reiner Siebert, Reinhard Schneppenheim

Journal:

Genes, Chromosomes and Cancer

Year:

2010

Language:

english

File:

PDF, 84 KB

english, 2010

5

Denosumab: a potential new and innovative treatment option for aneurysmal bone cysts

Lange, Tobias, Stehling, Christoph, FrÃ¶hlich, Birgit, KlingenhÃ¶fer, Mark, Kunkel, Philip, Schneppenheim, Reinhard, Escherich, Gabriele, Gosheger, Georg, Hardes, Jendrik, JÃ¼rgens, Heribert, Schulte,

Journal:

European Spine Journal

Year:

2013

Language:

english

File:

PDF, 418 KB

english, 2013

6

Williams-Beuren syndrome 35 years after the diagnosis in one of the first Beuren patients

Pankau, Rainer, Partsch, Carl-Joachim, Gosch, Angela, Siebert, Reiner, Schneider, Manfred, Schneppenheim, Reinhard, Winter, Martin, Wessel, Armin

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 94 KB

english, 2000

7

Williams-Beuren-Syndrom Spätdiagnose bei einem 24jährigen Mann

R. Pankau, C.-J. Partsch, Angela Gosch, M. Winter, R. Schneppenheim

Journal:

Monatsschrift Kinderheilkunde

Year:

1998

Language:

german

File:

PDF, 198 KB

german, 1998

8

Haemophilia A: from mutation analysis to new therapies

Graw, Jochen, Brackmann, Hans-Hermann, Oldenburg, Johannes, Schneppenheim, Reinhard, Spannagl, Michael, Schwaab, Rainer

Journal:

Nature Reviews Genetics

Year:

2005

Language:

english

File:

PDF, 689 KB

english, 2005

9

Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw–Schulman Syndrome Investigated in Germany

Hassenpflug, Wolf, Obser, Tobias, Bode, Julia, Oyen, Florian, Budde, Ulrich, Schneppenheim, Sonja, Schneppenheim, Reinhard, Brehm, Maria

Journal:

Thrombosis and Haemostasis

Year:

2018

Language:

english

File:

PDF, 571 KB

english, 2018

10

Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion

Langer, F., Obser, T., Oyen, F., Spath, B., Holstein, K., Greinacher, A., White, J. G., Budde, U., Bokemeyer, C., Schneppenheim, R.

Journal:

Thrombosis and Haemostasis

Year:

2013

Language:

english

File:

PDF, 2.24 MB

english, 2013

11

The extraordinary challenge of treating patients with congenital rhabdoid tumors-a collaborative European effort

Nemes, Karolina, Clément, Nathalie, Kachanov, Denis, Bens, Susanne, Hasselblatt, Martin, Timmermann, Beate, Schneppenheim, Reinhard, Gerss, Joachim, Siebert, Reiner, Furtwängler, Rhoikos, Bourdeaut, F

Journal:

Pediatric Blood & Cancer

Year:

2018

Language:

english

File:

PDF, 483 KB

english, 2018

12

Asymptomatischer Thrombus in der Pulmonalarterie Heterozygote Resistenz gegen aktiviertes Protein C (APC-Resistenz)

Liane Krienke, M. Hofbeck, R. Schneppenheim, M. Ries, H. Singer, H. Segerer

Journal:

Monatsschrift Kinderheilkunde

Year:

1999

Language:

german

File:

PDF, 290 KB

german, 1999

13

The mutation spectrum of the facilitative glucose transporter geneSLC2A2 (GLUT2)in patients with Fanconi-Bickel syndrome

René Santer, Sebastian Groth, Martina Kinner, Anja Dombrowski, Gerard T. Berry, Johannes Brodehl, James V. Leonard, Shimon Moses, Svante Norgren, Flemming Skovby, Reinhard Schneppenheim, Beat Steinman

Journal:

Year:

2002

Language:

english

File:

PDF, 61 KB

english, 2002

14

The intramembrane protease SPPL2a promotes B cell development and controls endosomal traffic by cleavage of the invariant chain

Schneppenheim, J., Dressel, R., Huttl, S., Lullmann-Rauch, R., Engelke, M., Dittmann, K., Wienands, J., Eskelinen, E.-L., Hermans-Borgmeyer, I., Fluhrer, R., Saftig, P., Schroder, B.

Journal:

Journal of Experimental Medicine

Year:

2013

Language:

english

File:

PDF, 3.44 MB

english, 2013

15

The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe

René Santer, Johannes Rischewski, Michaela von Weihe, Marko Niederhaus, Sonja Schneppenheim, Kurt Baerlocher, Alfried Kohlschütter, Ania Muntau, Hans-Georg Posselt, Beat Steinmann, Reinhard Schneppenh

Journal:

Year:

2005

Language:

english

File:

PDF, 162 KB

english, 2005

16

Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome

René Santer, Martina Kinner, Marie Passarge, Andrea Superti-Furga, Ertan Mayatepek, Thomas Meissner, Reinhard Schneppenheim, Jürgen Schaub

Journal:

Year:

2001

Language:

english

File:

PDF, 129 KB

english, 2001

17

Coagulation and fibrinolysis in children with APC-resistance: a population study

U. Nowak-Göttl, H. Vielhaber, R. Schneppenheim, H.G. Koch

Journal:

Fibrinolysis and Proteolysis

Year:

1996

Language:

english

File:

PDF, 242 KB

english, 1996

18

P26 Pregnancy in Upshaw Schulman Syndrome

K. Kentouche, A. Voigt, U. Budde, R. Schneppenheim, J. Beck, E. Schleussner

Journal:

Thrombosis Research

Year:

2009

Language:

english

File:

PDF, 52 KB

english, 2009

19

Left Ventricular Hypertrophy and Diastolic Dysfunction in Healthy Pregnant Women

Schannwell, Christiana M., Zimmermann, Tobias, Schneppenheim, Markus, Plehn, Gunnar, Marx, Roger, Strauer, Bodo E.

Journal:

Year:

2002

Language:

english

File:

PDF, 81 KB

english, 2002

20

Recurrent mutation of JAK3 in T-cell prolymphocytic leukemia

Bergmann, Anke K., Schneppenheim, Sina, Seifert, Marc, Betts, Matthew J., Haake, Andrea, Lopez, Cristina, Maria Murga Penas, Eva, Vater, Inga, Jayne, Sandrine, Dyer, Martin J.S., Schrappe, Martin, Düh

Journal:

Genes, Chromosomes and Cancer

Year:

2014

Language:

english

File:

PDF, 441 KB

english, 2014

21

Obituary.

Baldauf, Carsten, Obser, Tobias, Pieconka, Antje, Schneppenheim, Sonja, Budde, Ulrich, Schneppenheim, Reinhard, Graeter, Frauke

Journal:

Year:

1916

Language:

english

File:

PDF, 211 KB

english, 1916

22

Clinical Characteristics and Outcome of Children with Extracranial, Extrarenal Rhabdoid Tumors Registered to the European Rhabdoid Registry 2007–2013

Bartelheim, K., Seeringer, A., Leuschner, I., Schenk, J.P., Timmermann, B., Rübe, C., Graf, N., Koscielniak, E., Schneppenheim, R., Siebert, R., Frühwald, M.C.

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 56 KB

english, 2014

23

Distinct mechanisms account for acquired von Willebrand syndrome in plasma cell dyscrasias

Dicke, Christina, Schneppenheim, Sonja, Holstein, Katharina, Spath, Brigitte, Bokemeyer, Carsten, Dittmer, Rita, Budde, Ulrich, Langer, Florian

Journal:

Annals of Hematology

Year:

2016

Language:

english

File:

PDF, 856 KB

english, 2016

24

Detection of SMARCB1 loss in ascites cells in the diagnosis of an abdominal rhabdoid tumor

Kerl, Kornelius, Oyen, Florian, Leuschner, Ivo, Schneppenheim, Reinhard, Nagel, Inga, Siebert, Reiner, Groll, Andreas H., Hartmann, Wolfgang, Barth, Peter Josef, Bartelheim, Kerstin, Seringer, Angela,

Journal:

Pediatric Blood & Cancer

Year:

2015

Language:

english

File:

PDF, 1.26 MB

english, 2015

25

Inflammation-associated ADAMTS13 deficiency promotes formation of ultra-large von Willebrand factor

Bockmeyer, C. L., Claus, R. A., Budde, U., Kentouche, K., Schneppenheim, R., Losche, W., Reinhart, K., Brunkhorst, F. M.

Journal:

Year:

2008

Language:

english

File:

PDF, 282 KB

english, 2008

26

11 Hemophilia A Patients without Mutations in the Factor VIII Encoding Gene

Klopp, N., Oldenburg, J., Uen, C., Schneppenheim, R., Graw, J.

Journal:

Thrombosis and Haemostasis

Year:

2002

Language:

english

File:

PDF, 189 KB

english, 2002

27

Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations

König, Gesa, Obser, Tobias, Marggraf, Olivier, Schneppenheim, Sonja, Budde, Ulrich, Schneppenheim, Reinhard, Brehm, Maria

Journal:

Thrombosis and Haemostasis

Year:

2019

Language:

english

File:

PDF, 505 KB

english, 2019

28

Ins405AsnPro Mutation in the von Willebrand Factor Propeptide in Recessive Type 2A (IIC) von Willebrand’s Disease

Holmberg, L., Karpman, D., Isaksson, C., Kristoffersson, A. C., Lethagen, S., Schneppenheim, R.

Journal:

Thrombosis and Haemostasis

Year:

1998

Language:

english

File:

PDF, 72 KB

english, 1998

29

Alles fließt?

Schneppenheim, Reinhard, Brehm, Maria Alexandra

Journal:

Biologie in unserer Zeit

Year:

2019

Language:

german

File:

PDF, 1.43 MB

german, 2019

30

Angeborene Gerinnungsstörungen – Unterarmgangrän bei „normaler“ Gerinnung

Blohm, M., Lehmberg, K., Schrum, J., Helmke, K., Ridderbusch, I., Schneppenheim, R., Singer, D.

Journal:

Zeitschrift für Geburtshilfe und Neonatologie

Year:

2016

Language:

german

File:

PDF, 182 KB

german, 2016

31

Thrombosis and Haemostasis [Schattauer GmbH XIth International Congress on Thrombosis and Haemostasis - Brussels, Belgium (1987.07.06-1987.07.10)] XIth International Congress on Thrombosis and Haemostasis - LUMINOGRAPHIC VISUALIZATION OF VON WILLEBRAND FACTOR MULTIMERS

Schneppenheim, R, Plendl, H, Budde, U

Year:

1987

File:

PDF, 92 KB

1987

32

Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome

Schneppenheim, Reinhard, Dombrowski, Anja, Götze, Hermann, Steinmann, Beat, Schaub, Jürgen, Santer, René

Journal:

Nature Genetics

Year:

1997

File:

PDF, 560 KB

1997

33

High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors

Hasselblatt, Martin, Isken, Sarah, Linge, Anna, Eikmeier, Kristin, Jeibmann, Astrid, Oyen, Florian, Nagel, Inga, Richter, Julia, Bartelheim, Kerstin, Kordes, Uwe, Schneppenheim, Reinhard, Frühwald, Mi

Journal:

Genes, Chromosomes and Cancer

Year:

2013

Language:

english

File:

PDF, 335 KB

english, 2013

34

Characterisation of mutations and molecular studies of type 2 von Willebrand disease

Ahmad, F., Jan, R., Kannan, M., Obser, T., Hassan, M. I., Oyen, F., Budde, U., Saxena, R., Schneppenheim, R.

Journal:

Thrombosis and Haemostasis

Year:

2012

Language:

english

File:

PDF, 2.18 MB

english, 2012

35

Prognostic Value of Clinical, Histopathological and Molecular Features in AT/RT

Hasselblatt, Martin, Brokinkel, Benjamin, Bartelheim, Kerstin, Schneppenheim, Reinhard, Siebert, Reiner, Frühwald, Michael

Journal:

Cancer Genetics

Year:

2014

Language:

english

File:

PDF, 37 KB

english, 2014

36

Inherited Thrombotic Thrombocytopenic Purpura (Upshaw Schulman Syndrome) as Differential Diagnosis to Neonatal Septicaemia with Disseminated Intravascular Coagulation – a Case Series

Lehmberg, K., Hassenpflug, W., Klaassen, I., Hillebrand, G., Oyen, F., Budde, U., Singer, D., Schneppenheim, R.

Journal:

Zeitschrift für Geburtshilfe und Neonatologie

Year:

2016

Language:

english

File:

PDF, 342 KB

english, 2016

37

Diagnose der thrombotischthrombozytopenischen Purpura

Budde, U., Angerhaus, D., Obser, T., Schneppenheim, R.

Journal:

Hämostaseologie

Year:

2004

File:

PDF, 114 KB

2004

38

Identification of a candidate missense mutation in a family with von Willebrand disease type IIC

Reinhard Schneppenheim, Kathy B. Thomas, Sonja Krey, Ulrich Budde, Ursula Jessat, Anton H. Sutor, Barbara Zieger

Journal:

Year:

1995

Language:

english

File:

PDF, 833 KB

english, 1995

39

Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population

A. MOHL, Z. BODA, R. JAGER, H. LOSONCZY, A. MAROSI, T. MASSZI, E. NAGY, L. NEMES, T. OBSER, F. OYEN, G. RADVÁNYI, Á. SCHLAMMADINGER, ZS. SZÉLESSY, A. VÁRKONYI, K. VEZENDY, B. VILIMI, R. SCHNEPPENHEIM,

Journal:

Journal of Thrombosis and Haemostasis

Year:

2011

Language:

english

File:

PDF, 152 KB

english, 2011

40

Left ventricular diastolic function in physiologic and pathologic hypertrophy

Christiana M. Schannwell, Markus Schneppenheim, Gunnar Plehn, Roger Marx, Bodo E. Strauer

Journal:

American Journal of Hypertension

Year:

2002

Language:

english

File:

PDF, 79 KB

english, 2002

41

Remission of thrombotic thrombocytopenic purpura in a patient with compound heterozygous deficiency of von Willebrand factor-cleaving protease by infusion of solvent/detergent plasma

Kentouche, K., Budde, U., Furlan, M., Scharfe, V., Schneppenheim, R., Zintl, F.

Journal:

Acta Paediatrica

Year:

2002

Language:

english

File:

PDF, 162 KB

english, 2002

42

Feasibility of Intensive Multimodal Therapy in Infants Affected by Rhabdoid Tumors – Experience of the EU-RHAB registry

Seeringer, A., Bartelheim, K., Kerl, K., Hasselblatt, M., Leuschner, I., Rutkowski, S., Timmermann, B., Kortmann, R.-D., Koscielniak, E., Schneppenheim, R., Warmuth-Metz, M., Gerß, J., Siebert, R., Gr

Journal:

Klinische Pädiatrie

Year:

2014

File:

PDF, 242 KB

2014

43

Paraneoplastic Cerebellar Degeneration in Pediatric Hodgkin Disease

Hahn, A., Claviez, A., Brinkmann, G., Altermatt, H. J., Schneppenheim, R., Stephani, U.

Journal:

Neuropediatrics

Year:

2000

File:

PDF, 843 KB

2000

44

Mechano-Induced Unfolding of Von Willebrand Factor: A Clinical Example of Protein Destabilization

Aponte Santamaria, Camilo A., Lippok, Svenja, Mittag, Judith J., Obser, Tobias, Schneppenheim, Reinhard, Baldauf, Carsten, Gräter, Frauke, Budde, Ulrich, Rädler, Joachim

Journal:

Biophysical Journal

Year:

2017

Language:

english

File:

PDF, 42 KB

english, 2017

45

Comparison of von Willebrand factor plateletâbinding activity assays: ELISA overreads type 2B with loss of HMW multimers

Szederjesi, Attila, Baronciani, Luciano, Budde, Ulrich, Castaman, Giancarlo, Colpani, Paola, Lawrie, Andrew S., Liu, Yuan, Montgomery, Robert, Peyvandi, Flora, Schneppenheim, Reinhard, Patzke, JÃ¼rgen

Journal:

Journal of Thrombosis and Haemostasis

Year:

2020

File:

PDF, 12.02 MB

2020

46

Parvovirus B19 infection and autoimmune hepatitis in a child with sickle cell anemia

Uwe Kordes, Reinhard Schneppenheim, Andrea Briem-Richter, Stefanie Scherpe, Hans-Jörg Schäfer

Journal:

Pediatric Blood & Cancer

Year:

2011

Language:

english

File:

PDF, 101 KB

english, 2011

47

Tumorwachstum und Nebenniere 1

Huhn, Fr. O., Schneppenheim, P., Strake, H.

Journal:

DMW - Deutsche Medizinische Wochenschrift

Year:

1956

Language:

german

File:

PDF, 194 KB

german, 1956

48

Quantification and Facilitated Comparison of von Willebrand Factor Multimer Patterns by Densitometry

Studt, Jan D., Budde, Ulrich, Schneppenheim, Reinhard, Eisert, Roswit, von Depka Prondzinski, Mario, Ganser, Arnold, Barthels, Monika

Journal:

American Journal of Clinical Pathology

Year:

2001

Language:

english

File:

PDF, 138 KB

english, 2001

49

Pregnancy in Upshaw-Schulman syndrome

Kentouche, K., Voigt, A., Schleussner, E., Schneppenheim, R., Budde, U., Beck, J. F., Stefanska-Windyga, E., Windyga, J.

Journal:

Hämostaseologie

Year:

2013

File:

PDF, 353 KB

2013

50

Die „Erosion“ der Portio

H. Hamperl, C. Kaufmann, K. G. Ober, P. Schneppenheim

Journal:

Virchows Archiv

Year:

1958

Language:

german

File:

PDF, 2.51 MB

german, 1958

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