Kate Kernan

None None 2 collaborations

Amy J LaCroix 1 collaboration

Deborah Stabley 1 collaboration

Rebecca Sahraoui 1 collaboration

Margaret P Adam 1 collaboration

Michele Mehaffey 1 collaboration

Kelly Kernan 1 collaboration

Candace T Myers 1 collaboration

Carrie Fagerstrom 1 collaboration

George Anadiotis 1 collaboration

Yassmine M Akkari 1 collaboration

Katherine M Robbins 1 collaboration

Karen W Gripp 1 collaboration

Wagner A R Baratela 1 collaboration

Michael B Bober 1 collaboration

Angela L Duker 1 collaboration

Dan Doherty 1 collaboration

Jennifer C Dempsey 1 collaboration

Daniel G Miller 1 collaboration

Martin Kircher 1 collaboration

Michael J Bamshad 1 collaboration

Deborah A Nickerson 1 collaboration

Heather C Mefford 1 collaboration

Katia Sol-Church 1 collaboration

Bita Shakoory 1 collaboration

Ashley Geerlinks 1 collaboration

Marta Wilejto 1 collaboration

Melissa Hines 1 collaboration

Micol Romano 1 collaboration

David Piskin 1 collaboration

Angelo Ravelli 1 collaboration

Rashmi Sinha 1 collaboration

Daniel Aletaha 1 collaboration

Carl Allen 1 collaboration

Hamid Bassiri 1 collaboration

Edward M Behrens 1 collaboration

Joseph Carcillo 1 collaboration

Linda Carl 1 collaboration

Winn Chatham 1 collaboration

Jeffrey I Cohen 1 collaboration

Randy Q Cron 1 collaboration

Erik Drewniak 1 collaboration

Alexei A Grom 1 collaboration

Lauren A Henderson 1 collaboration

Annacarin Horne 1 collaboration

Michael B Jordan 1 collaboration

Kim E Nichols 1 collaboration

Grant Schulert 1 collaboration

Sebastiaan Vastert 1 collaboration

Erkan Demirkaya 1 collaboration

Raphaela Goldbach-Mansky 1 collaboration

Fabrizio de Benedetti 1 collaboration

Rebecca A Marsh 1 collaboration

Scott W Canna 1 collaboration

Affiliations

Publications (2)

GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome.

The 2022 EULAR/ACR points to consider at the early stages of diagnosis and management of suspected haemophagocytic lymphohistiocytosis/macrophage activation syndrome (HLH/MAS).

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