SCOPUS 정보 검색 플랫폼

Journal of Gastroenterology

Volumn 40, Issue 8, 2005, Pages 859-860

Hypertransaminasemia: The end of a thread

(1) Matsui, Akira a

a UNIVERSITY OF TSUKUBA (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; GAMMA GLUTAMYLTRANSFERASE;

ALANINE AMINOTRANSFERASE BLOOD LEVEL; ASPARTATE AMINOTRANSFERASE BLOOD LEVEL; CHILDHOOD DISEASE; CONGENITAL DISORDER OF GLYCOSYLATION; DIFFERENTIAL DIAGNOSIS; EARLY DIAGNOSIS; EDITORIAL; ENZYME ASSAY; FAMILY; GENETIC DISORDER; HISTOPATHOLOGY; HUMAN; HYPERTRANSAMINASEMIA; LIVER DISEASE; LIVER FUNCTION TEST; PREVALENCE; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SMITH LEMLI OPITZ SYNDROME; STEATOSIS; WILSON DISEASE;

BIOLOGICAL MARKERS; CHILD; GENETIC DISEASES, INBORN; HUMANS; LIVER DISEASES; TRANSAMINASES;

EID: 25144443121 PISSN: 09441174 EISSN: 14355922 Source Type: Journal
DOI: 10.1007/s00535-005-1675-z Document Type: Editorial

Times cited : (9)

References (12)

1
- 25144508019
- Serum glutamic oxalacetic aminopherase (transaminase) in hepatitis
- 13295080
- F Wroblewski JS Ladue 1956 Serum glutamic oxalacetic aminopherase (transaminase) in hepatitis J Am Med Assoc 160 1130-1134 13295080
- (1956) J. Am. Med. Assoc. , vol.160 , pp. 1130-1134
- Wroblewski, F.¹ Ladue, J.S.²

2
- 78651031427
- Serum glutamic pyruvic transaminase in cardiac with hepatic disease
- 13323003
- F Wroblewski JS Ladue 1956 Serum glutamic pyruvic transaminase in cardiac with hepatic disease Proc Soc Exp Biol Med 91 569-571 13323003
- (1956) Proc. Soc. Exp. Biol. Med. , vol.91 , pp. 569-571
- Wroblewski, F.¹ Ladue, J.S.²

3
- 0022263441
- Persistent hypertransaminasemia as the presenting finding of childhood muscle disease
- J Rutledge J Andersen CW Fink J Cook A Strickland 1985 Persistent hypertransaminasemia as the presenting finding of childhood muscle disease Clin Pediatr (Phila) 24 500-503
- (1985) Clin. Pediatr. (Phila) , vol.24 , pp. 500-503
- Rutledge, J.¹ Andersen, J.² Fink, C.W.³ Cook, J.⁴ Strickland, A.⁵

4
- 0004866707
- Lippincott Williams & Wilkins Philadelphia
- LA Batres ES Maller 2001 Laboratory assessment of liver function and injury in children Lippincott Williams & Wilkins Philadelphia
- (2001) Laboratory Assessment of Liver Function and Injury in Children
- Batres, L.A.¹ Maller, E.S.²

5
- 0003468454
- 3rd ed. Butterworth-Heinemann Oxford
- A Mowat 1994 Liver disorders in childhood 3rd ed. Butterworth-Heinemann Oxford
- (1994) Liver Disorders in Childhood
- Mowat, A.¹

6
- 25144445813
- Hypertranaminasemia in childhood as a marker of genetic liver disorders
- R Iorio A Sepe A Giannattasio F Cirillo A Vegnente 2005 Hypertranaminasemia in childhood as a marker of genetic liver disorders J Gastroenterol 40 820-826
- (2005) J. Gastroenterol. , vol.40 , pp. 820-826
- Iorio, R.¹ Sepe, A.² Giannattasio, A.³ Cirillo, F.⁴ Vegnente, A.⁵

7
- 0030135839
- Chronic idiopathic hypertransaminasemia
- 8926957
- L Zancan T Bettiol A Rini R Giacchino P Gandullia P Vajro 1996 Chronic idiopathic hypertransaminasemia Minerva Pediatr 48 209-216 8926957
- (1996) Minerva Pediatr. , vol.48 , pp. 209-216
- Zancan, L.¹ Bettiol, T.² Rini, A.³ Giacchino, R.⁴ Gandullia, P.⁵ Vajro, P.⁶

8
- 19944429834
- Characterization of liver involvement in defects of cholesterol biosynthesis: Long-term follow-up and review
- 10.1002/ajmg.a.30426
- M Rossi P Vajro R Iorio A Battagliese N Brunetti-Pierri G Corso 2005 Characterization of liver involvement in defects of cholesterol biosynthesis: Long-term follow-up and review Am J Med Genet 132 144-151 10.1002/ajmg.a.30426
- (2005) Am. J. Med. Genet. , vol.132 , pp. 144-151
- Rossi, M.¹ Vajro, P.² Iorio, R.³ Battagliese, A.⁴ Brunetti-Pierri, N.⁵ Corso, G.⁶

9
- 13944271954
- Congenital disorder of glycosylation type Ia revealed by hypertransaminasemia and failure to thrive in a young boy with normal neurodevelopment
- 10.1097/00005176-200502000-00030 15699704
- C Pancho A Garcia-Cazorla V Varea R Artuch I Ferrer MA Vilaseca 2005 Congenital disorder of glycosylation type Ia revealed by hypertransaminasemia and failure to thrive in a young boy with normal neurodevelopment J Pediatr Gastroenterol Nutr 40 230-232 10.1097/ 00005176-200502000-00030 15699704
- (2005) J. Pediatr. Gastroenterol. Nutr. , vol.40 , pp. 230-232
- Pancho, C.¹ Garcia-Cazorla, A.² Varea, V.³ Artuch, R.⁴ Ferrer, I.⁵ Vilaseca, M.A.⁶

10
- 14644429791
- Hypertran-saminasemia superior a 400 U/l en adultos atendidos en un hospital terciario. Estudio prospectivo de su etiologia
- 10.1157/13077764 15691463
- M Bruguera JM Barrera F Corradi A Mas 2005 Hypertran-saminasemia superior a 400 U/l en adultos atendidos en un hospital terciario. Estudio prospectivo de su etiologia. (Hypertransaminasemia greater than 400 U/l in adults seen at a tertiary hospital. Prospective study of etiology Gastroenterol Hepatol 28 15-19 10.1157/13077764 15691463
- (2005) Gastroenterol. Hepatol. , vol.28 , pp. 15-19
- Bruguera, M.¹ Barrera, J.M.² Corradi, F.³ Mas, A.⁴

11
- 0017036179
- Sibling cases of chronic recurrent hepatocerebral disease with hypercitrullinemia
- 1017595
- T Tsujii T Morita Y Matsuyama T Matsui M Tamura Y Matsuoka 1976 Sibling cases of chronic recurrent hepatocerebral disease with hypercitrullinemia Gastroenterol Jpn 11 328-340 1017595
- (1976) Gastroenterol. Jpn. , vol.11 , pp. 328-340
- Tsujii, T.¹ Morita, T.² Matsuyama, Y.³ Matsui, T.⁴ Tamura, M.⁵ Matsuoka, Y.⁶

12
- 0033767770
- Hereditary hemochromatosis
- 11109593
- S Durupt I Durieu R Nove-Josserand L Bencharif H Rousset D Vital Durand 2000 Hereditary hemochromatosis Rev Med Interne 21 961-971 11109593
- (2000) Rev. Med. Interne. , vol.21 , pp. 961-971
- Durupt, S.¹ Durieu, I.² Nove-Josserand, R.³ Bencharif, L.⁴ Rousset, H.⁵ Vital Durand, D.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.