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Koschmieder, Ingo
20  results:
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1

Determination of absolute size of fundus objects:

Dawczynski, Jens ; Gebhardt, Michael ; Mohr, Thomas...
Graefe's Archive for Clinical and Experimental Ophthalmology.  249 (2010)  3 - p. 381-387 , 2010
Link: https://doi.org/10.1007/..
 
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2

Bilddiagnostik der Netzhaut mit der Funduskamera:

Koschmieder, Ingo ; Müller, Lothar
Zeitschrift für Medizinische Physik.  17 (2007)  1 - p. 67-72 , 2007
Link: https://doi.org/10.1016/..
 
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3

Verbundvorhaben Ophthalmoinnovation Thüringen (OIT) 

Teilvorhaben: Light Adjust Technology (LAT) ; Abschlussberi... 
Gerlach, Mario ; Koschmieder, Ingo , [ca. 2006]
Link: http://edok01.tib.uni-ha..
 
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4

Identification of Adult Patients With Classical Dyskeratosi..:

Tometten, Mareike ; Kirschner, Martin ; Meyer, Robert...
HemaSphere.  7 (2023)  5 - p. e874 , 2023
Link: https://doi.org/10.1097/..
 
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5

Novel homozygous nonsense mutation in the P5′N‐1 coding gen..:

Kirschner, Martin ; Heinen, Inga Rebecca ; Koschmieder, Steffen...
Clinical Case Reports.  10 (2022)  3 - p. , 2022
Link: https://doi.org/10.1002/..
 
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6

Evaluation of Chiral Organosulfur Compounds on Their Activi..:

Ngwa, Che ; Stratmann, Rabea ; Musabyimana, Jean...
Tropical Medicine and Infectious Disease.  7 (2022)  12 - p. 416 , 2022
Link: https://doi.org/10.3390/..
 
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7

Germline variants in DNA repair genes, including BRCA1/2, m..:

Elbracht, Miriam ; Meyer, Robert ; Kricheldorf, Kim...
Blood Advances.  5 (2021)  17 - p. 3373-3376 , 2021
Link: https://doi.org/10.1182/..
 
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8

Loss of supervillin causes myopathy with myofibrillar disor..:

Hedberg-Oldfors, Carola ; Meyer, Robert ; Nolte, Kay...
Brain.  143 (2020)  8 - p. 2406-2420 , 2020
Link: https://doi.org/10.1093/..
 
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9

Recurrent somatic mutations are rare in patients with crypt..:

Kirschner, Martin ; Maurer, Angela ; Wlodarski, Marcin W....
Leukemia.  32 (2018)  8 - p. 1762-1767 , 2018
Link: https://doi.org/10.1038/..
 
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10

Identification of Adult Patients With Classical Dyskeratosi..:

Tometten, Mareike ; Kirschner, Martin ; Meyer, Robert...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10121438/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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11

Evaluation of Chiral Organosulfur Compounds on Their Activi..:

Che, Julius Ngwa ; Stratmann, Rabea ; Pradel, Gabriele...
info:eu-repo/semantics/altIdentifier/wos/WOS:000902682600001.  , 2022
Link: https://publications.rwt..
 
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12

Novel homozygous nonsense mutation in the P5′N-1 coding gen..:

Kirschner, Martin ; Heinen, Inga Rebecca ; Koschmieder, Steffen...
info:eu-repo/semantics/altIdentifier/doi/10.18154/RWTH-CONV-249536.  , 2022
Link: https://publications.rwt..
 
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13

Novel homozygous nonsense mutation in the P5′N‐1 coding gen..:

Kirschner, Martin ; Heinen, Inga Rebecca ; Koschmieder, Steffen...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895901/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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14

Germline variants in DNA repair genes, including BRCA1/2, m..:

Elbracht, Miriam ; Meyer, Robert ; Kricheldorf, Kim...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525218/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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15

Loss of supervillin causes myopathy with myofibrillar disor..:

Hedberg-Oldfors, Carola ; Meyer, Robert ; Nolte, Kay...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447519/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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