Helicobacter pylori - Portal Neonatal

44. Beaulieu JF. Differential expression of the VLA family of
integrins along the crypt–villus axis in the human small
intestine. J Cell Sci 1992; 102: 427–436.
45. Simon-Assmann P, Duclos B, Orian-Rousseau V et al.
Differential expression of laminin isoforms and a6-b4
integrin subunits in the developing human and mouse
intestine. Dev Dynamics 1994; 201: 71–85.
46. Simon-Assmann P, Bouziges F, Vigny M, Kedinger M.
Origin and deposition of basement membrane. Heparan
sulfate proteoglycan in the developing intestine. J Cell
Biol 1989; 109: 1837–1848.
47. Simo P, Simon-Assmann P, Bouziges F et al. Changes in
the expression of laminin during intestinal development.
Development 1991; 112: 477–487.
48. Simo P, Bouziges F, Lissitzky JC et al. Dual and asynchronous
deposition of laminin chains at the epithelial
mesenchymal interface in the gut. Gastroenterology
1992; 102: 1835–1845.
49. Simon-Assmann P, Kedinger M. Heterotypic cellular
cooperation in gut morphogenesis and differentiation.
Cell Biol 1993; 4: 221–230.
50. Cameron DJS, Barnes GL. Successful pregnancy
outcome in tufting enteropathy. J Pediatr Gastroenterol
Nutr 2003; 36: 158.
51. Lacaille F, Cuenod B, Colomb V et al. Successful
combined liver and small bowel transplantation in a
child with epithelial dysplasia. J Pediatr Gastroenterol
Nutr 1998; 2: 230–233.
52. Goulet O. Intestinal transplantation. Curr Opin Clin
Nutr Metab Care 1999; 2: 315–321.
53. Paramesh AS, Fishbein T, Tschernia A et al. Isolated
small bowel transplantation for tufting enteropathy. J
Pediatr Gastroenterol Nutr 2003; 36: 138–140.
54. Verloes A, Lombet J, Lambert Y et al. Tricho-hepatoenteric
syndrome: further delineation of a distinct
syndrome with neonatal hemochromatosis phenotype,
intractable diarrhea, and hair anomalies. Am J Med Gen
1997; 68: 391–395.
References 11
55. De Vries E, Visser DM, Van Dongen JJ et al. Oligoclonal
gammopathy in ‘phenotypic diarrhea’. J Pediatr
Gastroenterol Nutr 2000; 30: 349–350
56. Cormier-Daire V, Bonnefont JP, Rustin P et al.
Mitochondrial DNA rearrangements with onset as
chronic diarrhea with villus atrophy. J Pediatr 1994;
124: 63–70.
57. Murch S, Winyard PJD, Koletzko S et al. Congenital
enterocyte heparan sulphate deficiency with massive
albumin loss, secretory diarrhoea and malnutrition.
Lancet 1996; 347: 1299–1301.
58. Jaeken J, Matthijs G, Saudubray JM et al.
Phosphomannose isomerase deficiency: a carbohydratedeficient
glycoprotein syndrome with hepatic–intestinal
presentation. Am J Hum Genet 1998; 62: 1535–1539.
59. Oren A, Houwen RH. Phosphomannose isomerase deficiency
as the cause of protein-losing enteropathy and
congenital liver fibrosis. J Pediatr Gastroenterol Nutr
1999; 29: 231–232.
60. Smith LJ, Szymanski W, Foulston C et al. Familial
enteropathy with villus edema and immunoglobulin G2
subclass deficiency. J Pediatr 1994; 125: 541–548.
61. Itin PH, Pittelkow MR. Trichothiodystrophy: review of
sulfur-deficient brittle hair syndromes and association
with the ectodermal dysplasia. J Am Acad Dermatol
1990; 22: 705–717.
62. Happle R, Traupe H, Gröbe H, Bonsmann G. The Tay
syndrome (congenital ichthyosis with trichothiodystrophy).
Eur J Pediatr 1984; 141: 147–152.
63. Stefanini M, Vermeulen W, Weeda G et al. A new
nucleotide-excision-repair gene associated with the
disorder trichothiodystrophy. Am J Hum Genet 1993; 53:
817–821.
64. Mariani E, Facchini A, Honorati MC et al. Immune
defects in families and patients with xeroderma pigmentosum
and trichothiodystrophy. Clin Exp Immunol 1992;
88: 376–382.