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Female [MeSH]
[x]
Sacherschließung
Humans [MeSH]
(6)
Male [MeSH]
(3)
Brain Neoplasms/genetics [MeSH]
(2)
Young Adult [MeSH]
(1)
X-linked Nuclear Protein/genetics [MeSH]
(1)
Unusual phenotype
(1)
Transcription Factors/genetics [MeSH]
(1)
Time Factors [MeSH]
(1)
Thioguanine/administration
(1)
Publikationstyp
Artikel
(6)
Erscheinungsjahr
2021
(4)
2020
(2)
Institution
6 Treffer
Kurzansicht
E-Jahr
Zugriff
Typ
Operations
Hepatic sinusoidal obstruction syndrome and short-term application of 6-thioguanine in pediatric acute lymphoblastic leukemia
2021 .
Stanulla, Martin
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Schaeffeler, Elke
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Möricke, Anja
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Buchmann, Swantje
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Zimmermann, Martin
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Igel, Svitlana
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Schmiegelow, Kjeld
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Flotho, Christian
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Hartmann, Hans
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Illsinger, Sabine
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Sauerbrey, Axel
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Junk, Stefanie V.
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Schütte, Peter
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Hinze, Laura
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Lauten, Melchior
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Modlich, Simon
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Kolb, Reinhard
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Rossig, Claudia
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Schwabe, Georg
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Gnekow, Astrid K.
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Fleischhack, Gudrun
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Schlegel, Paul Gerhard
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Schünemann, Holger J.
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Kratz, Christian P.
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Cario, Gunnar
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Schrappe, Martin
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Schwab, Matthias
2021
http://purl.org/ontology/bibo/Article
Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li–Fraumeni syndrome
2021 .
Winter, Greta
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Kirschner-Schwabe, Renate
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Groeneveld-Krentz, Stefanie
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Escherich, Gabriele
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Möricke, Anja
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von Stackelberg, Arend
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Stanulla, Martin
|
Bailey, Simon
|
Richter, Lisa
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Steinemann, Doris
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Ripperger, Tim
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Escudero, Adela
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Farah, Roula
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Lohi, Olli
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Wadt, Karin
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Jongmans, Marjolijn
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van Engelen, Nienke
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Eckert, Cornelia
|
Kratz, Christian
2021
http://purl.org/ontology/bibo/Article
Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group
2021 .
Frühwald, Michael
|
Nemes, K.
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Boztug, H.
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Cornips, M. C. A.
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Evans, Gareth
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farah, roula
|
Glentis, Stavros
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Jorgensen, M.
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Katsibardi, Katerina
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Hirsch, Steffen
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Jahnukainen, K.
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kventsel, iris
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Kerl, Kornelius
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Kratz, Christian
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Pajtler, Kristian W.
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Kordes, Uwe R.
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Ridola, Vita
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Stutz, E.
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BOURDEAUT, Franck
2021
http://purl.org/ontology/bibo/Article
Unusual phenotypes in patients with a pathogenic germline variant in DICER1
2021 .
Venger, Kateryna
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Elbracht, Miriam
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Carlens, Julia
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Deutz, Peter
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Zeppernick, Felix
|
Lassay, Lisa
|
Kratz, Christian
|
Zenker, Martin
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Kim, Jung
|
Stewart, Douglas R.
|
Wieland, Ilse
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Schultz, Kris Ann P.
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Schwerk, Nicolaus
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Kurth, Ingo
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Kontny, Udo
2021
http://purl.org/ontology/bibo/Article
Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important
2020 .
Eggermann, Thomas
|
Brück, Johanna
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Knopp, Cordula
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Fekete, György
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Kratz, Christian
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Tasic, Velibor
|
Kurth, Ingo
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Elbracht, Miriam
|
Eggermann, Katja
|
Begemann, Matthias
2020
http://purl.org/ontology/bibo/Article
Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis
2020 .
Suwala, Abigail K.
|
Stichel, Damian
|
Schrimpf, Daniel
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Kloor, Matthias
|
Wefers, Annika K.
|
Reinhardt, Annekathrin
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Maas, Sybren L. N.
|
Kratz, Christian P.
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Schweizer, Leonille
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Hasselblatt, Martin
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Snuderl, Matija
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Abedalthagafi, Malak Sameer J.
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Abdullaev, Zied
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Monoranu, Camelia M.
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Bergmann, Markus
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Pekrun, Arnulf
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Freyschlag, Christian
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Aronica, Eleonora
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Kramm, Christof M.
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Hinz, Felix
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Sievers, Philipp
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Korshunov, Andrey
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Kool, Marcel
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Pfister, Stefan M.
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Sturm, Dominik
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Jones, David T. W.
|
Wick, Wolfgang
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Unterberg, Andreas
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Hartmann, Christian
|
Dodgshun, Andrew
|
Tabori, Uri
|
Wesseling, Pieter
|
Sahm, Felix
|
von Deimling, Andreas
|
Reuß, David
2020
http://purl.org/ontology/bibo/Article