Suchergebnisse - "Perry, David J"

PubPharm (101)

1

The Delphi and GRADE methodology used in the PSOGI 2018 consensus statement on Pseudomyxoma Peritonei and Peritoneal Mesothelioma

enthalten in: European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology | 2021

von Lurvink, R. | Villeneuve, L. | Govaerts, K. | +78

2

Rare case of hepatocellular carcinoma metastasising to the pituitary and cavernous sinus causing panhypopituitarism and bilateral ophthalmoplegia

enthalten in: BMJ case reports | 2020

von Ambalavanan, J. | Peravali, M. | Perry, D.

3

Increased infection rates associated with tetracycline therapy given for epidermal growth factor receptor inhibitor (EGFRI)-associated acneiform eruption : A retrospective study of data from two cancer centers

enthalten in: Journal of the American Academy of Dermatology | 2020

von Magnino, M. | Perry, D. | Subramaniam, D. | +1

4

Next-generation sequencing for the diagnosis of MYH9-RD : Predicting pathogenic variants

enthalten in: Human mutation | 2020

von Bury, L. | Megy, K. | Stephens, J. | +34

5

Next‐generation sequencing for the diagnosis of MYH9‐RD : Predicting pathogenic variants

enthalten in: Human mutation | 2020

von Bury, L. | Megy, K. | Stephens, J. | +34

6

Laboratory assay measurement of modified clotting factor concentrates : a review of the literature and recommendations for practice

enthalten in: Journal of thrombosis and haemostasis : JTH | 2019

von Young, G. | Perry, D. | International Prophylaxis Study Group (IPSG)

7

Laboratory assay measurement of modified clotting factor concentrates : a review of the literature and recommendations for practice

enthalten in: Journal of Thrombosis and Haemostasis | 2019

von Young, G. | Perry, D.

8

Publisher Correction : Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

enthalten in: Scientific reports | 2018

von Farmery, J. | Smith, M. | NIHR BioResource - Rare Diseases | +101

ErratumFor: Sci Rep. 2018 Jan 22;8(1):1300. - PMID 29358629

9

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

enthalten in: American journal of human genetics | 2018

von Ito, Y. | Carss, K. | Duarte, S. | +118

10

Telomerecat : A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

enthalten in: Scientific reports | 2018

von Farmery, J. | Smith, M. | NIHR BioResource - Rare Diseases | +101

ErratumIn: Sci Rep. 2018 Sep 3;8(1):13376. - PMID 30177810

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