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1 sionally causes frequent and crippling acute neurovisceral attacks associated with increased hepatic
2 terized clinically by skin lesions and acute neurovisceral attacks that occur separately or together.
3 A) and porphobilinogen (PBG) promotes sudden neurovisceral attacks, which can be life-threatening.
5 iemann-Pick Type C1 (NPC1) disease is a rare neurovisceral, cholesterol-sphingolipid lysosomal storag
7 use of Niemann-Pick type C2 disease, a fatal neurovisceral disorder characterized by accumulation of
8 iemann-Pick type C1 (NPC1) disease is a rare neurovisceral disorder characterized by intracellular ac
9 Niemann-Pick type C (NP-C) disease, a fatal neurovisceral disorder, is characterized by lysosomal ac
11 n-Pick type C disease (NP-C) is an inherited neurovisceral lipid storage disorder characterized by pr
12 iemann-Pick disease type C (NPC) is a severe neurovisceral lysosomal storage disorder caused by defec
14 s between the presence of out-group members, neurovisceral reactions, religiosity, and ethnocentrism,
15 or Batten disease, the most common inherited neurovisceral storage disease of childhood, was identifi
16 e C (NP-C) disease is an autosomal recessive neurovisceral storage disorder in which cholesterol and
17 synthesis, cause life-threatening attacks of neurovisceral symptoms that mimic many other acute medic
18 hese disorders present clinically with acute neurovisceral symptoms which may be sporadic or recurren
21 sified as follows: (1) acute porphyrias with neurovisceral symptoms: acute intermittent porphyria; de
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