Microvillous inclusion disease in Japan [1]

Journal of Pediatrics

Volumn 135, Issue 3, 1999, Pages 400-

  Kaneko, K ^a   Shimizu, T ^a   Fujiwara, S ^a   Igarashi, J ^a   Ohtamo, Y ^a   Yamashiro, Y ^a  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; INCIDENCE; JAPAN; LETTER; MALE; MEDICAL LITERATURE; MICROVILLUS; MICROVILLUS INCLUSION DISEASE; NEWBORN; PRIORITY JOURNAL; UNITED KINGDOM;

EID: 0033505877     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(99)70146-0     Document Type: Letter

References (4)

1. JF Pohl MD Shub EE Trevelline A cluster of microvillous inclusion disease in the Navajo population J Pediatr 134 1999 103 106
2. A Satoh Y Matsumoto K Matuzaki A case of congenital microvillous atrophy (Japanese) J Jpn Pediatr Soc 94 1990 1661 1666
3. K Kagitani K Miki Y Etani A case of congenital microvillous atrophy complicated by hyperphosphatemic rickets during long-term total parenteral nutrition [in Japanese]. Abstracts of the 23rd Annual Meeting of the Japanese Society for Pediatric Gastroenterology and Nutrition 1996 121
4. J Igarashi T Shimizu K Kaneko A sibling of congenital microvillous atrophy [in Japanese]. Abstracts of the 25th Annual Meeting of the Japanese Society for Pediatric Gastroenterology and Nutrition 1998 80