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Bamborschke, Daniel
9  Ergebnisse:
Personensuche X
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1

The phenotypic spectrum of PCDH12 associated disorders - Fi..:

Fazeli, Walid ; Bamborschke, Daniel ; Moawia, Abubakar...
European Journal of Paediatric Neurology.  36 (2022)  - p. 7-13 , 2022
Link: https://doi.org/10.1016/..
 
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2

PNPT1 mutations may cause Aicardi-Goutières-Syndrome:

Bamborschke, Daniel ; Kreutzer, Mona ; Koy, Anne...
Brain and Development.  43 (2021)  2 - p. 320-324 , 2021
Link: https://doi.org/10.1016/..
 
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3

Genotype-phenotype correlations in ocular manifestations of..:

Bayram, Nurettin ; Kaçar Bayram, Ayşe ; Daimagüler, Hülya-Sevcan...
European Journal of Ophthalmology.  32 (2021)  3 - p. NP92-NP97 , 2021
Link: https://doi.org/10.1177/..
 
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4

Mutation in CEP135 causing primary microcephaly and subcort..:

Bamborschke, Daniel ; Daimagüler, Hülya‐Sevcan ; Hahn, Andreas...
American Journal of Medical Genetics Part A.  182 (2020)  10 - p. 2450-2453 , 2020
Link: https://doi.org/10.1002/..
 
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5

Ultra‐rapid emergency genomic diagnosis of Donahue syndrome..:

Bamborschke, Daniel ; Özdemir, Özkan ; Kreutzer, Mona...
American Journal of Medical Genetics Part A.  185 (2020)  1 - p. 90-96 , 2020
Link: https://doi.org/10.1002/..
 
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6

A novel mutation in sphingosine-1-phosphate lyase causing c..:

Bamborschke, Daniel ; Pergande, Matthias ; Becker, Kerstin...
Brain and Development.  40 (2018)  6 - p. 480-483 , 2018
Link: https://doi.org/10.1016/..
 
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7

Genetische Ursachen des Steroidresistenten Nephrotischen Sy..:

Bamborschke, Daniel , 2017
Link: http://nbn-resolving.de/..
 
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8

The phenotypic spectrum of PCDH12 associated disorders - fi..:

Fazeli, Walid ; Bamborschke, Daniel ; Moawia, Abubakar...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939053/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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9

Rapid Response to Cyclosporin A and Favorable Renal Outcome..:

Büscher, Anja K ; Beck, Bodo B ; Melk, Anette...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741047/.  , 2016
Link: http://www.ncbi.nlm.nih...
 
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