Suchergebnisse - "Rodenburg, R J"

PubPharm (116)

1

Skeletal muscle toxicity associated with tyrosine kinase inhibitor therapy in patients with chronic myeloid leukemia

enthalten in: Leukemia | 2019

von Janssen, L. | Frambach, S. | Allard, N. | +6

2

Tivozanib for the treatment of renal cell carcinoma : patient selection and perspectives

enthalten in: International journal of nephrology and renovascular disease | 2019

von Rodenburg, R. | Eskens, F.

3

Validation of the Chowdhury overall survival score in patients with melanoma brain metastasis treated with Gamma Knife Radiosurgery

enthalten in: Journal of neuro-oncology | 2018

von Rodenburg, R. | Hanssens, P. | Ho, V. | +1

4

QIL1-dependent assembly of MICOS complex-lethal mutation in C19ORF70 resulting in liver disease and severe neurological retardation

enthalten in: Journal of human genetics | 2018

von Gödiker, J. | Grüneberg, M. | DuChesne, I. | +10

5

Mining for mitochondrial mechanisms : Linking known syndromes to mitochondrial function

enthalten in: Clinical genetics | 2018

von Panneman, D. | Smeitink, J. | Rodenburg, R.

6

Validation of the Chowdhury overall survival score in patients with melanoma brain metastasis treated with Gamma Knife Radiosurgery

enthalten in: Journal of neuro-oncology | 2018

von Rodenburg, R. | Hanssens, P. | Ho, V. | +1

7

Validation of the Chowdhury overall survival score in patients with melanoma brain metastasis treated with Gamma Knife Radiosurgery

enthalten in: Journal of neuro-oncology | 2018

von Rodenburg, R. | Hanssens, P. | Ho, V. | +1

8

Validation of the Chowdhury overall survival score in patients with melanoma brain metastasis treated with Gamma Knife Radiosurgery

enthalten in: Journal of neuro-oncology | 2018

von Rodenburg, R. | Hanssens, P. | Ho, V. | +1

9

NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect

enthalten in: Clinical genetics | 2018

von Baertling, F. | Sánchez-Caballero, L. | van den Brand, M. | +8

10

Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions

enthalten in: Human genetics | 2017

von Renkema, G. | Visser, G. | Baertling, F. | +8

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