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Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients
Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients
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Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients

DÖRK, Thilo ; BENDIX, Regina ; WEISE, Sabine ; STUHRMANN, Manfred ; KARSTENS, Johann H ; BREMER, Michael ; RADES, Dirk ; KLÖPPER, Karin ; NICKE, Marion ; SKAWRAN, Britta ; HECTOR, Ariadne ; YAMINI, Paria ; STEINMANN, Diana

Cancer research (Chicago, Ill.), 2001-10, Vol.61 (20), p.7608-7615 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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2
Vascular endothelial growth factor A polymorphism and risk of Kaposi's sarcoma herpesvirus viremia in kidney allograft recipients
Vascular endothelial growth factor A polymorphism and risk of Kaposi's sarcoma herpesvirus viremia in kidney allograft recipients
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Vascular endothelial growth factor A polymorphism and risk of Kaposi's sarcoma herpesvirus viremia in kidney allograft recipients

Alkharsah, K.R. ; Alzahrani, A.J. ; Obeid, O.E. ; El-Harith, E.-H.A. ; Guella, A. ; Mohamed, E.A. ; Haykal, A.H. ; Stuhrmann, M. ; Al-Ali, A.K.

Transplant infectious disease, 2014-10, Vol.16 (5), p.783-789 [Periódico revisado por pares]

Denmark: Blackwell Publishing Ltd

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3
Augmentation Index and the Evolution of Aortic Disease in Marfan-Like Syndromes
Augmentation Index and the Evolution of Aortic Disease in Marfan-Like Syndromes
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Augmentation Index and the Evolution of Aortic Disease in Marfan-Like Syndromes

Mortensen, Kai ; Baulmann, Johannes ; Rybczynski, Meike ; Sheikhzadeh, Sara ; Aydin, Muhammet A. ; Treede, Henrik ; Dombrowski, Ellen ; Kühne, Kristin ; Peitsmeier, Philipp ; Habermann, Christian R. ; Robinson, Peter N. ; Stuhrmann, Manfred ; Berger, Jürgen ; Meinertz, Thomas ; von Kodolitsch, Yskert

American journal of hypertension, 2010-07, Vol.23 (7), p.716-724 [Periódico revisado por pares]

Basingstoke: Oxford University Press

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4
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens
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Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens

DÖRK, T ; DWORNICZAK, B ; PANDER, H.-J ; SPERLING, H ; RATJEN, F ; PASSARGE, E ; SCHMIDTKE, J ; STUHRMANN, M ; AULEHLA-SCHOLZ, C ; WIECZOREK, D ; BÖHM, I ; MAYEROVA, A ; SEYDEWITZ, H. H ; NIESCHLAG, E ; MESCHEDE, D ; HORST, J

Human genetics, 1997-09, Vol.100 (3-4), p.365-377 [Periódico revisado por pares]

Heidelberg: Springer

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5
Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy
Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy
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Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy

Senderek, Jan ; Bergmann, Carsten ; Stendel, Claudia ; Kirfel, Jutta ; Verpoorten, Nathalie ; De Jonghe, Peter ; Timmerman, Vincent ; Chrast, Roman ; Verheijen, Mark H.G. ; Lemke, Greg ; Battaloglu, Esra ; Parman, Yesim ; Erdem, Sevim ; Tan, Ersin ; Topaloglu, Haluk ; Hahn, Andreas ; Müller-Felber, Wolfgang ; Rizzuto, Nicolò ; Fabrizi, Gian Maria ; Stuhrmann, Manfred ; Rudnik-Schöneborn, Sabine ; Züchner, Stephan ; Michael Schröder, J. ; Buchheim, Eckhard ; Straub, Volker ; Klepper, Jörg ; Huehne, Kathrin ; Rautenstrauss, Bernd ; Büttner, Reinhard ; Nelis, Eva ; Zerres, Klaus

American journal of human genetics, 2003-11, Vol.73 (5), p.1106-1119 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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6
Genetic predisposition for a compromised immune system after multiple trauma
Genetic predisposition for a compromised immune system after multiple trauma
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Genetic predisposition for a compromised immune system after multiple trauma

HILDEBRAND, Frank ; PAPE, Hans-Christoph ; VAN GRIENSVEN, Martijn ; MEIER, Sven ; HASENKAMP, Sandra ; KRETTEK, Christian ; STUHRMANN, Manfred

Shock (Augusta, Ga.), 2005-12, Vol.24 (6), p.518-522 [Periódico revisado por pares]

Augusta, GA: BioMedical Press

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7
Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia
Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia
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Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia

Brakensiek, K ; Frye-Boukhriss, H ; Mälzer, M ; Abramowicz, M ; Bahr, MJ ; Von Beckerath, N ; Bergmann, C ; Caselitz, M ; Holinski-Feder, E ; Muschke, P ; Oexle, K ; Strobl-Wildemann, G ; Wolff, G ; El-Harith, EA ; Stuhrmann, M

Clinical genetics, 2008-08, Vol.74 (2), p.171-177 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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8
Familial thrombocytosis as a recessive, possibly X‐linked trait in an Arab family
Familial thrombocytosis as a recessive, possibly X‐linked trait in an Arab family
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Familial thrombocytosis as a recessive, possibly X‐linked trait in an Arab family

Stuhrmann, M ; Bashawri, L. ; Ahmed, M. A. ; Al‐Awamy, B. H. ; Kühnau, W. ; Schmidtke, J. ; El‐Harith, E. A.

British journal of haematology, 2001-03, Vol.112 (3), p.616-620 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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9
Frequency of BRCA1 Mutation 5382insC in German Breast Cancer Patients
Frequency of BRCA1 Mutation 5382insC in German Breast Cancer Patients
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Frequency of BRCA1 Mutation 5382insC in German Breast Cancer Patients

Backe, Jael ; Hofferbert, Sigrun ; Skawran, Britta ; Dörk, Thilo ; Stuhrmann, Manfred ; Karstens, Johann H. ; Untch, Michael ; Meindl, Alfons ; Burgemeister, Renate ; Chang-Claude, Jenny ; Weber, Bernhard H.F.

Gynecologic oncology, 1999-03, Vol.72 (3), p.402-406 [Periódico revisado por pares]

San Diego, CA: Elsevier Inc

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10
Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease
Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease
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Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease

METZGER, Silke ; BAUER, Peter ; SEPPI, Klaus ; MELEGH, Bela ; HAVASI, Viktoria ; BALIKO, Laszlo ; WIECZOREK, Stefan ; ZAREMBA, Jacek ; HOFFMAN-ZACHARSKA, Dorota ; SULEK, Anna ; NAZLI BASAK, A ; SOYDAN, Esra ; TOMIUK, Jürgen ; ZIDOVSKA, Jana ; KEBRDLOVA, Vera ; PANDOLFO, Massimo ; RIBÏ, Pascale ; KADASI, Ludovit ; KVASNICOVA, Marta ; WEBER, Bernhard H. F ; KREUZ, Friedmar ; DOSE, Matthias ; STUHRMANN, Manfred ; LACCONE, Franco ; RIESS, Olaf ; DIDONATO, Stefano ; GELLERA, Cinzia ; MARIOTTI, Caterina ; LANGE, Herwig W ; WEIRICH-SCHWAIGER, Helga ; WENNING, Gregor K

Human genetics, 2006-09, Vol.120 (2), p.285-292 [Periódico revisado por pares]

Heidelberg: Springer

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