전문정보검색
| No | 제목 / 내용 |
|---|---|
| 1 |
A Single F153Sβ3 Mutation Causes Constitutive Integrin αIIbβ3 Activation in a Variant Form of This report identifies a novel variant form of the inherited bleeding disorder, Glanzmann thrombasthenia (GT) exhibiting only mild in |
| 2 |
A Single F153Sβ3 Mutation Causes Constitutive Integrin αIIbβ3 Activation in a Variant Form of This report identifies a novel variant form of the inherited bleeding disorder, Glanzmann thrombasthenia (GT) exhibiting only mild ble |
| 3 |
A Single F153Sβ3 Mutation Causes Constitutive Integrin αIIbβ3 Activation in a Variant Form of This report identifies a novel variant form of the inherited bleeding disorder, Glanzmann thrombasthenia (GT) exhibiting only mild ble |
| 4 |
NCOG-34. A DESCRIPTIVE ANALYSIS OF GLIOMATOSIS CEREBRI CASES, COMPARED ACCORDING TO IDH STATUS 1 2 3 4 7 a (5 10 16 19 3+ 43 GC II IV Of On RT as at be by is no of on or to 3/7 6/7 AA, All GC, IDH Ten The age all and had our the |
| 5 |
NCOG-34. A DESCRIPTIVE ANALYSIS OF GLIOMATOSIS CEREBRI CASES, COMPARED ACCORDING TO IDH STATUS 1 2 3 4 7 a (5 10 16 19 3+ 43 GC II IV Of On RT as at be by is no of on or to 3/7 6/7 AA, All GC, IDH Ten The age all and had our the |
| 6 |
NCOG-39. EXPLORING PATIENT REPORTED OUTCOMES (PROS) ACROSS ETHNORACIAL GROUPS IN PRIMARY BRAIN T ( = a p (p 5% 50 6% AA be in is no of on or to 10% 28% 29% 40% 44% 562 79% AND KPS PBT The age all and but for had has may not per the |
| 7 |
NCOG-39. EXPLORING PATIENT REPORTED OUTCOMES (PROS) ACROSS ETHNORACIAL GROUPS IN PRIMARY BRAIN T ( = a p (p 5% 50 6% AA be in is no of on or to 10% 28% 29% 40% 44% 562 79% AND KPS PBT The age all and but for had has may not per the |