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Dahl, Hans-Henrik M.
~ 200  results:
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1

Kufs disease due to mutation ofCLN6: clinical, pathological..:

Berkovic, Samuel F ; Oliver, Karen L ; Canafoglia, Laura...
Brain.  142 (2018)  1 - p. 59-69 , 2018
Link: https://doi.org/10.1093/..
 
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2

Diagnosis and misdiagnosis of adult neuronal ceroid lipofus..:

Berkovic, Samuel F. ; Staropoli, John F. ; Carpenter, Stirling...
Neurology.  87 (2016)  6 - p. 579-584 , 2016
Link: https://doi.org/10.1212/..
 
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3

Evaluation of multiple putative risk alleles within the 15q..:

Damiano, John A. ; Mullen, Saul A. ; Hildebrand, Michael S....
Epilepsy Research.  117 (2015)  - p. 70-73 , 2015
Link: https://doi.org/10.1016/..
 
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4

Mutation of the nuclear lamin geneLMNB2in progressive myocl..:

Damiano, John A. ; Afawi, Zaid ; Bahlo, Melanie...
Human Molecular Genetics.  24 (2015)  16 - p. 4483-4490 , 2015
Link: https://doi.org/10.1093/..
 
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5

16p11.2 600 kb Duplications confer risk for typical and aty..:

Reinthaler, Eva M. ; Lal, Dennis ; Lebon, Sebastien...
Human Molecular Genetics.  23 (2014)  22 - p. 6069-6080 , 2014
Link: https://doi.org/10.1093/..
 
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6

Etiology and Audiological Outcomes at 3 Years for 364 Child..:

Dahl, Hans-Henrik M. ; Ching, Teresa Y. C. ; Hutchison, Wendy...
PLoS ONE.  8 (2013)  3 - p. e59624 , 2013
Link: https://doi.org/10.1371/..
 
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7

Eeyore: A Novel Mouse Model of Hereditary Deafness:

Miller, Kerry A. ; Williams, Louise H. ; Dahl, Hans-Henrik M...
PLoS ONE.  8 (2013)  9 - p. e74243 , 2013
Link: https://doi.org/10.1371/..
 
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8

Characterization of a novel ENU-generated myosin VI mutant ..:

Williams, Louise H. ; Miller, Kerry A. ; Dahl, Hans-Henrik M..
Hearing Research.  299 (2013)  - p. 53-62 , 2013
Link: https://doi.org/10.1016/..
 
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9

Epilepsy, hippocampal sclerosis and febrile seizures linked..:

Kasperavičiūtė, Dalia ; Catarino, Claudia B. ; Matarin, Mar...
Brain.  136 (2013)  10 - p. 3140-3150 , 2013
Link: https://doi.org/10.1093/..
 
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10

Inner Ear Morphology Is Perturbed in Two Novel Mouse Models..:

Miller, Kerry A. ; Williams, Louise H. ; Rose, Elizabeth...
PLoS ONE.  7 (2012)  12 - p. e51284 , 2012
Link: https://doi.org/10.1371/..
 
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11

A Mutation in Synaptojanin 2 Causes Progressive Hearing Los..:

Manji, Shehnaaz S. M. ; Williams, Louise H. ; Miller, Kerry A....
PLoS ONE.  6 (2011)  3 - p. e17607 , 2011
Link: https://doi.org/10.1371/..
 
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12

Advances in Molecular and Cellular Therapies for Hearing Lo..:

Hildebrand, Michael S ; Newton, Stephen S ; Gubbels, Samuel P...
Molecular Therapy.  16 (2008)  2 - p. 224-236 , 2008
Link: https://doi.org/10.1038/..
 
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13

A reduction of mitochondrial DNA molecules during embryogen..:

Cree, Lynsey M ; Samuels, David C ; de Sousa Lopes, Susana Chuva...
Nature Genetics.  40 (2008)  2 - p. 249-254 , 2008
Link: https://doi.org/10.1038/..
 
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14

A novel splice site mutation inEYA4 causes DFNA10 hearing l..:

Hildebrand, Michael S. ; Coman, David ; Yang, Tao...
American Journal of Medical Genetics Part A.  143A (2007)  14 - p. 1599-1604 , 2007
Link: https://doi.org/10.1002/..
 
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15

Gene expression profiling analysis of the inner ear:

Hildebrand, Michael S. ; de Silva, Michelle G. ; Klockars, Tuomas...
Hearing Research.  225 (2007)  1-2 - p. 1-10 , 2007
Link: https://doi.org/10.1016/..
 
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