Researcher
MD PhD Associate Professor in Neurology Andreas Puschmann
Skånes universitetssjukhus Lund (Skåne University Hospital, Lund)
Statistics
5 papers found
All papers authored by MD PhD Associate Professor in Neurology Andreas Puschmann
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2022
Hector Garcia‐Moreno 
,
Mercedes Prudencio ,
Gilbert Thomas‐Black ,
Nita Solanky ,
Karen R. Jansen‐West ,
Rana Hanna AL‐Shaikh ,
Amanda Heslegrave ,
Henrik Zetterberg ,
Magda M. Santana ,
Luis Pereira de Almeida ,
Ana Vasconcelos‐Ferreira ,
Cristina Januário,
Jon Infante ,
Jennifer Faber ,
Thomas Klockgether
and 12 other authors
,
Mercedes Prudencio ,
Gilbert Thomas‐Black ,
Nita Solanky ,
Karen R. Jansen‐West ,
Rana Hanna AL‐Shaikh ,
Amanda Heslegrave ,
Henrik Zetterberg ,
Magda M. Santana ,
Luis Pereira de Almeida ,
Ana Vasconcelos‐Ferreira ,
Cristina Januário,
Jon Infante ,
Jennifer Faber ,
Thomas Klockgether
and 12 other authors
Tau and neurofilament light‐chain as fluid biomarkers in spinocerebellar ataxia type 3
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2020
Mercedes Prudencio ,
Hector Garcia-Moreno ,
Karen R. Jansen-West ,
Rana Hanna Al-Shaikh ,
Tania F. Gendron ,
Michael G. Heckman,
Matthew R. Spiegel,
Yari Carlomagno ,
Lillian M. Daughrity ,
Yuping Song,
Judith A. Dunmore ,
Natalie Byron,
Björn Oskarsson ,
Katharine A. Nicholson,
Nathan P. Staff
and 37 other authors
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,
Hector Garcia-Moreno ,
Karen R. Jansen-West ,
Rana Hanna Al-Shaikh ,
Tania F. Gendron ,
Michael G. Heckman,
Matthew R. Spiegel,
Yari Carlomagno ,
Lillian M. Daughrity ,
Yuping Song,
Judith A. Dunmore ,
Natalie Byron,
Björn Oskarsson ,
Katharine A. Nicholson,
Nathan P. Staff
and 37 other authors
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2018
Josef Davidsson,
Andreas Puschmann ,
Ulf Tedgård ,
David Bryder,
Lars Nilsson,
Jörg Cammenga
,
Ulf Tedgård ,
David Bryder,
Lars Nilsson,
Jörg Cammenga
SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies
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2014
Emil Ygland,
Franco Taroni,
Cinzia Gellera ,
Serena Caldarazzo,
Morten Duno,
Maria Soller,
Andreas Puschmann
,
Serena Caldarazzo,
Morten Duno,
Maria Soller,
Andreas Puschmann
Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis
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