Family of a Patient with Serum Cholinesterase Deficiency.
スポンサーリンク
概要
- 論文の詳細を見る
A-39-year-old man was admitted to our hospital because of a markedly decreased level of serum cholinesterase found incidentally by a blood test. Detailed examination did not reveal severe liver disease, malignant tumor, infection or organophosphate compound poisoning. Investigation of three generations of his family revealed two homozygous and five heterozygous family members with the cholinesterase deficiency gene E1s indicating familial serum cholinesterase deficiency.(Internal Medicine 31 : 397-399, 1992)
- 社団法人 日本内科学会の論文
著者
-
IMAI Masanobu
the Department of Internal Medicine, Mitoyo General Hospital
-
Hirohata Mamoru
The Department Of Internal Medicine Mitoyo General Hospital
-
Imai Masanobu
The Department Of Internal Medicine Mitoyo General Hospital
-
Hirasaki Shoji
The Department Of Internal Medicine
-
KUMASHIRO Hirofumi
the Department of Internal Medicine, Mitoyo General Hospital
-
OKAMOTO Ryoichi
the Department of Internal Medicine, Mitoyo General Hospital
-
MIYATANI Hiroyuki
the Department of Internal Medicine, Mitoyo General Hospital
-
OHARA Masaki
the Department of Internal Medicine, Mitoyo General Hospital
-
TOSHIMORI Tsukasa
the Department of Internal Medicine, Mitoyo General Hospital
-
MORITANI Hiroki
the Department of Internal Medicine, Mitoyo General Hospital
-
TOMINAGA Yokoh
the Department of Internal Medicine, Mitoyo General Hospital
関連論文
- Churg-Strauss Syndrome with Pleural Involvement
- Pulmonary Lymphangiomyomatosis (LAM) Developing Chylothorax
- Peripheral Arterial Coil Embolization for Hepatic Arteriovenous Malformation in Osler-Weber-Rendu Disease ; Useful for Controlling High Output Heart Failure, but Harmful to the Liver
- A Family with Hereditary Serum Cholinesterase Deficiency
- Family of a Patient with Serum Cholinesterase Deficiency.