Results 11 to 20 of about 144,103 (203)
Reviewer acknowledgements [PDF]
Discern wishes to acknowledge the following individuals for their assistance with peer review of manuscripts for this issue. Their contribution towards the quality of the journal is greatly appreciated. Lisa Elzey Mercer, University of Illinois, Urbana-
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Reviewer acknowledgements [PDF]
Discern wishes to acknowledge the following individuals for their assistance with peer review of manuscripts for this issue. Their contribution to the quality of the journal is greatly appreciated.
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Reviewer Acknowledgements 2021
Reviewer Acknowledgements ...
Teresa Terrazas
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Reviewer Acknowledgement [PDF]
CONTRIBUTING REVIEWERS: The editors of Molecular Pain would like to thank all the reviewers who have contributed to the journal in Volume 8 (2012).
Gu, Jianguo, Zhuo, Min
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ABSTRACT Pediatric gastroenteropancreatic neuroendocrine neoplasms (GEP‐NENs) are extremely rare and clinically heterogeneous. Management has largely been extrapolated from adult practice. This European Standard Clinical Practice Guideline (ESCP), developed by the EXPeRT network in collaboration with adult NEN experts, provides (adult) evidence ...
Michaela Kuhlen +23 more
wiley +1 more source
ABSTRACT Background Children with sickle cell disease (SCD) face multiple acute and chronic medical complications that may impact their quality of life as reported by patients themselves. Health‐related social needs (HRSNs), such as food and housing insecurity, are common in people with SCD, but the association between HRSNs and patient‐reported ...
Sarah J. Marks +5 more
wiley +1 more source
ABSTRACT Cup‐like nuclei are a distinctive morphological feature observed in certain cases of acute lymphoblastic leukemia (ALL). We provide evidence that they characterize DUX4/ERG ALL independently of IKZF1 deletion and reveal marked mitochondrial accumulation in this ALL subset.
Chloé Arfeuille +9 more
wiley +1 more source
ABSTRACT Primary cutaneous anaplastic large cell lymphoma (pcALCL) is a rare pediatric CD30‐positive T‐cell lymphoproliferative disorder with an excellent prognosis, but its genomic drivers are poorly defined. We report three children with skin‐limited disease demonstrating striking molecular heterogeneity, including NPM::ALK, NUP214::FRK, and a novel ...
Shoshana Greenberger +7 more
wiley +1 more source

