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Chahrokh-Zadeh, S.
12  results:
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1

A novel pathogenic CACNA1A variant causing episodic ataxia ..:

Penkava, Josef ; Ledderose, S. ; Chahrokh-Zadeh, S....
Journal of Neurology.  267 (2020)  S1 - p. 181-184 , 2020
Link: https://doi.org/10.1007/..
 
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2

Markedly different course of Friedreich's ataxia in sib pai..:

Klopstock, T. ; Chahrokh-Zadeh, S. ; Holinski-Feder, E....
Acta Neuropathologica.  97 (1999)  2 - p. 139-142 , 1999
Link: https://doi.org/10.1007/..
 
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3

The acid lipase gene family: three enzymes, one highly cons..:

Lohse, P ; Lohse, P ; Chahrokh-Zadeh, S.
Journal of Lipid Research.  38 (1997)  5 - p. 880-891 , 1997
Link: https://doi.org/10.1016/..
 
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4

Human lysosomal acid lipase/cholesteryl ester hydrolase and..:

Lohse, P ; Chahrokh-Zadeh, S ; Lohse, P.
Journal of Lipid Research.  38 (1997)  5 - p. 892-903 , 1997
Link: https://doi.org/10.1016/..
 
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5

Human lysosomal acid lipase/cholesteryl ester hydrolase and..:

Lohse, P ; Lohse, P ; Chahrokh-Zadeh, S.
Journal of Lipid Research.  38 (1997)  9 - p. 1896-1905 , 1997
Link: https://doi.org/10.1016/..
 
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6

A novel pathogenic CACNA1A variant causing episodic ataxia ..:

Penkava, Josef ; Ledderose, S ; Chahrokh-Zadeh, S...
https://repository.publisso.de/resource/frl:6469760.  , 2020
Link: https://repository.publi..
 
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7

FRAXE testing:

Holinski-Feder, E ; Chahrokh-Zadeh, S ; Jedele, K. B...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1914838.  , 1996
Link: http://www.ncbi.nlm.nih...
 
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8

Human lysosomal acid lipase/cholesteryl ester hydrolase and..:

P Lohse ; S Chahrokh-Zadeh ; D Seidel
http://www.sciencedirect.com/science/article/pii/S002222752037214X.  , 1997
Link: https://doi.org/10.1016/..
 
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9

The acid lipase gene family: three enzymes, one highly cons..:

P Lohse ; S Chahrokh-Zadeh ; D Seidel
http://www.sciencedirect.com/science/article/pii/S0022227520372138.  , 1997
Link: https://doi.org/10.1016/..
 
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10

Human lysosomal acid lipase/cholesteryl ester hydrolase and..:

P Lohse ; S Chahrokh-Zadeh ; D Seidel
http://www.sciencedirect.com/science/article/pii/S0022227520371649.  , 1997
Link: https://doi.org/10.1016/..
 
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11

Activating MRAS mutations cause Noonan syndrome associated ..:

Motta, Marialetizia ; Sagi-Dain, Lena ; Krumbach, Oliver H F...
Human Molecular Genetics.  29 (2019)  11 - p. 1772-1783 , 2019
Link: https://doi.org/10.1093/..
 
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12

SCA2 trinucleotide expansion in German SCA patients:

Riess, Olaf ; Laccone, Franco A. ; Gispert, Suzana...
neurogenetics.  1 (1997)  1 - p. 59-64 , 1997
Link: https://doi.org/10.1007/..
 
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