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Clinical Genetics|February 2, 2018
Expanding the clinical and genetic spectra of NKX6-2-related disorderC Baldi, A M Bertoli-Avella, N Al-Sannaa, et al.
Chest|December 13, 2016
The Power of Flash Mob Research: Conducting a Nationwide Observational Clinical Study on Capillary Refill Time in a Single DayJelmer Alsma, Jan L C M van Saase, Prabath W B Nanayakkara, et al.
The Journal of Infectious Diseases|June 1, 1996
Hantavirus pulmonary syndrome: the first 100 US casesA S Khan, R F Khabbaz, L R Armstrong, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|June 28, 2012
[Two German Birth Cohorts: GINIplus and LISAplus]J Heinrich, I Brüske, M Schnappinger, et al.
Neuron|March 10, 1998
Persephin, a novel neurotrophic factor related to GDNF and neurturinJ Milbrandt, F J de Sauvage, T J Fahrner, et al.
The Lancet. Infectious Diseases|March 8, 2012
Acute liver failure, multiorgan failure, cerebral oedema, and activation of proangiogenic and antiangiogenic factors in a case of Marburg haemorrhagic feverJudith van Paassen, Martijn P Bauer, M Sesmu Arbous, et al.
United European Gastroenterology Journal|September 29, 2020
Faecal microbiota transplantation for Clostridioides difficile infection: Four years' experience of the Netherlands Donor Feces BankElisabeth M Terveer, Karuna Ew Vendrik, Rogier E Ooijevaar, et al.
Neurology|August 8, 2008
Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptomsT Schmitz-Hübsch, M Coudert, P Bauer, et al.
Electrophoresis|March 4, 2022
Global intercompany assessment of ICIEF platform comparability for the characterization of therapeutic proteinsSeth Madren, Will McElroy, Kristin Schultz-Kuszak, et al.
Neurology|August 12, 2011
The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up studyH Jacobi, P Bauer, P Giunti, et al.
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