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/vufind/Search/Results?lookfor=%22Kim%2C+Borahm%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Kim%2C+Borahm%22&type=Person&sort=year
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PubPharm (31)
1
Serial Detection of MYD88 L265P Mutation in the Aqueous Humor of a Patient with Vitreoretinal Lymphoma for Disease Monitoring
enthalten in:
Ocular immunology and inflammation
| 2021
von
Choi, S.
|
Shin, S.
|
Lee, S.
| +4
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2
Corrigendum to 'Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy' [Brain Dev. 42(6) (2020) 438-448
enthalten in:
Brain & development
| 2021
von
Na, J.
|
Shin, S.
|
Yang, D.
| +7
ErratumFor: Brain Dev. 2020 Jun;42(6):438-448. - PMID 32139178
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3
Impact of maternal engrafted cytomegalovirus-specific CD8+ T cells in a patient with severe combined immunodeficiency
enthalten in:
Clinical & translational immunology
| 2021
von
Koh, J.
|
Lee, S.
|
Kim, B.
| +8
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4
Impact of maternal engrafted cytomegalovirus‐specific CD8+ T cells in a patient with severe combined immunodeficiency
enthalten in:
Clinical & Translational Immunology
| 2021
von
Koh, J.
|
Lee, S.
|
Kim, B.
| +8
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5
The phenotype and treatment of SCN2A-related developmental and epileptic encephalopathy
enthalten in:
Epileptic disorders : international epilepsy journal with videotape
| 2020
von
Kim, H.
|
Yang, D.
|
Kim, S.
| +6
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6
Whole exome sequencing identifies mutational signatures of vitreoretinal lymphoma
enthalten in:
Haematologica
| 2020
von
Lee, J.
|
Kim, B.
|
Lee, H.
| +6
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7
Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia
enthalten in:
Scientific reports
| 2020
von
Kim, B.
|
Yun, W.
|
Lee, S.
| +5
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8
Genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression pattern
enthalten in:
Epilepsy research
| 2020
von
Lee, S.
|
Kim, S.
|
Kim, B.
| +5
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9
Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy
enthalten in:
Brain & development
| 2020
von
Na, J.
|
Shin, S.
|
Yang, D.
| +7
ErratumIn: Brain Dev. 2021 Jan;43(1):179. - PMID 33008655
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10
Clinical Implementation of Targeted Gene Sequencing for Malformation of Cortical Development
enthalten in:
Pediatric neurology
| 2020
von
Lee, S.
|
Kim, S.
|
Kim, B.
| +5
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Annals of laboratory medicine
4
Annals of hematology
3
BMC medical genomics
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Epilepsy research
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PloS one
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Epileptic disorders : international epilepsy jo...
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Frontiers in neurology
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The Journal of molecular diagnostics : JMD
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18
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11
Research Support, Non-U.S. Gov't
5
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4
Oncogene Proteins, Fusion
3
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3
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3
Next-generation sequencing
3
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3
next-generation sequencing
2
Developmental and epileptic encephalopathy
2
Sodium Channel Blockers
2
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1
149025-06-9
1
9007-49-2
1
APC
1
Acute lymphoblastic leukemia
1
Adenomatous Polyposis Coli Protein
1
Antibodies, Monoclonal
1
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Erscheinungszeitraum
13
2020-
18
2010-2019
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