Deficiency of substance P-immunoreactive nerve fibres in children with intractable constipation: A form of intestinal neuronal dysplasia

被引：23
作者：
Hutson, JM
Chow, CW
Hurley, MR
Uemura, S
Wheatley, JM
CattoSmith, AG
机构：
[1] ROYAL CHILDRENS HOSP,DEPT PATHOL ANAT,PARKVILLE,VIC 3052,AUSTRALIA
[2] ROYAL CHILDRENS HOSP,DEPT GASTROENTEROL,PARKVILLE,VIC 3052,AUSTRALIA
来源：
JOURNAL OF PAEDIATRICS AND CHILD HEALTH | 1997年 / 33卷 / 03期
关键词：
D O I：
10.1111/j.1440-1754.1997.tb01577.x
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页码：187 / 189
页数：3
相关论文
共 11 条
[1]   MYOINTESTINAL, NEUROINTESTINAL, GASTROINTESTINAL ENCEPHALOPATHY (MNGIE SYNDROME) DUE TO PARTIAL DEFICIENCY OF CYTOCHROME-C-OXIDASE - A NEW MITOCHONDRIAL MULTISYSTEM DISORDER [J].
BARDOSI, A ;
CREUTZFELDT, W ;
DIMAURO, S ;
FELGENHAUER, K ;
FRIEDE, RL ;
GOEBEL, HH ;
KOHLSCHUTTER, A ;
MAYER, G ;
RAHLF, G ;
SERVIDEI, S ;
VANLESSEN, G ;
WETTERLING, T .
ACTA NEUROPATHOLOGICA, 1987, 74 (03) :248-258
[2]  
CSURY L, 1995, PEDIATR SURG INT, V10, P441
[3]   SLOW TRANSIT CHRONIC CONSTIPATION (ARBUTHNOT LANES DISEASE) - AN IMMUNOHISTOCHEMICAL STUDY OF NEUROPEPTIDE-CONTAINING NERVES IN RESECTED SPECIMENS FROM THE LARGE-BOWEL [J].
DOLK, A ;
BRODEN, G ;
HOLMSTROM, B ;
JOHANSSON, C ;
SCHULTZBERG, M .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 1990, 5 (04) :181-187
[4]   PLURICHEMICAL TRANSMISSION AND CHEMICAL CODING OF NEURONS IN THE DIGESTIVE-TRACT [J].
FURNESS, JB ;
YOUNG, HM ;
POMPOLO, S ;
BORNSTEIN, JC ;
KUNZE, WAA ;
MCCONALOGUE, K .
GASTROENTEROLOGY, 1995, 108 (02) :554-563
[5]   THE MALONE ANTEGRADE CONTINENCE ENEMA [J].
GRIFFITHS, DM ;
MALONE, PS .
JOURNAL OF PEDIATRIC SURGERY, 1995, 30 (01) :68-71
[6]   Intractable constipation with a decrease in substance P-immunoreactive fibres: Is it a variant of intestinal neuronal dysplasia? [J].
Hutson, JM ;
Chow, CW ;
Borg, J .
JOURNAL OF PEDIATRIC SURGERY, 1996, 31 (04) :580-583
[7]   Is intestinal neuronal dysplasia a disorder of the neuromuscular junction? [J].
Kobayashi, H ;
Hirakawa, H ;
Puri, P .
JOURNAL OF PEDIATRIC SURGERY, 1996, 31 (04) :575-579
[8]   CLOSE LINKAGE WITH THE RET PROTOONCOGENE AND BOUNDARIES OF DELETION MUTATIONS IN AUTOSOMAL-DOMINANT HIRSCHSPRUNG DISEASE [J].
LUO, Y ;
CECCHERINI, I ;
PASINI, B ;
MATERA, I ;
BICOCCHI, MP ;
BARONE, V ;
BOCCIARDI, R ;
KAARIAINEN, H ;
WEBER, D ;
DEVOTO, M ;
ROMEO, G .
HUMAN MOLECULAR GENETICS, 1993, 2 (11) :1803-1808
[9]  
MEIERRUGE WA, 1995, PEDIATR SURG INT, V10, P447
[10]  
SCHARLI AF, 1995, PEDIATR SURG INT, V10, P440
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