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PubPharm (12)
1
Genetic testing in autoinflammatory diseases - past, current and future perspectives
enthalten in:
European journal of internal medicine
| 2022
von
Le Goueff, A.
|
Smits, G.
|
Delaunoy, M.
| +2
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2
Case Report of an Unusual Tumor in an Adult With a TP53 Germline Mutation
enthalten in:
Clinical lymphoma, myeloma & leukemia
| 2021
von
Castiaux, J.
|
Vandernoot, I.
|
Dallemagne, J.
| +6
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3
Middle interhemispheric variant of holoprosencephaly : First prenatal report of a ZIC2 missense mutation
enthalten in:
Clinical case reports
| 2020
von
Gounongbé, C.
|
Marangoni, M.
|
Gouder de Beauregard, V.
| +4
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4
Novel features of PIK3CA-Related Overgrowth Spectrum : Lesson from an aborted fetus presenting a de novo constitutional PIK3CA mutation
enthalten in:
European journal of medical genetics
| 2020
von
De Graer, C.
|
Marangoni, M.
|
Romnée, S.
| +5
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5
Middle interhemispheric variant of holoprosencephaly : First prenatal report of a ZIC2 missense mutation
enthalten in:
Clinical Case Reports
| 2020
von
Gounongbé, C.
|
Marangoni, M.
|
Gouder de Beauregard, V.
| +4
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6
Undetectable circulating tumor DNA (ctDNA) levels correlate with favorable outcome in metastatic melanoma patients treated with anti-PD1 therapy
enthalten in:
Journal of translational medicine
| 2019
von
Seremet, T.
|
Jansen, Y.
|
Planken, S.
| +11
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7
Undetectable circulating tumor DNA (ctDNA) levels correlate with favorable outcome in metastatic melanoma patients treated with anti-PD1 therapy
enthalten in:
Journal of translational medicine
| 2019
von
Seremet, T.
|
Jansen, Y.
|
Planken, S.
| +11
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8
Undetectable circulating tumor DNA (ctDNA) levels correlate with favorable outcome in metastatic melanoma patients treated with anti-PD1 therapy
enthalten in:
Journal of translational medicine
| 2019
von
Seremet, T.
|
Jansen, Y.
|
Planken, S.
| +11
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9
Detection of a Large Novel α-Thalassemia Deletion in an Autochthonous Belgian Family
enthalten in:
Hemoglobin
| 2019
von
Heireman, L.
|
Luyckx, A.
|
Schynkel, K.
| +5
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10
Case report : An infantile lethal form of Albright hereditary osteodystrophy due to a GNAS mutation
enthalten in:
Clinical case reports
| 2018
von
Leclercq, V.
|
Benoit, V.
|
Lederer, D.
| +6
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12
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12
E-Artikel
12
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Zeitschriftentitel
3
Journal of translational medicine
2
Clinical case reports
1
Clinical Case Reports
1
Clinical lymphoma, myeloma & leukemia
1
European journal of internal medicine
1
European journal of medical genetics
1
Hemoglobin
1
Melanoma research
1
PloS one
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Thema
6
Journal Article
5
Case Reports
3
BRAF/NRAS mutations monitoring
3
Circulating tumor DNA
3
Immunotherapy
3
Liquid biopsy
3
Metastatic melanoma
3
Monitoring
3
Translational research
2
Circulating Tumor DNA
2
DNA, Neoplasm
2
Programmed Cell Death 1 Receptor
2
Research Support, Non-U.S. Gov't
1
31YO63LBSN
1
9056-09-1
1
Albright's hereditary osteodystrophy
1
Antibodies, Monoclonal
1
Antibodies, Monoclonal, Humanized
1
Autoinflammatory diseases
1
BRAF protein, human
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Erscheinungszeitraum
5
2020-
7
2010-2019
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