PubRank

H S Heymans

Author PubWeight™ 93.22‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 [Gastroesophageal reflux in infants; recommendations for diagnosis and treatment]. Ned Tijdschr Geneeskd 1995 2.30
2 Peroxisomal disorders: a newly recognised group of genetic diseases. Eur J Pediatr 1986 2.05
3 [Systematic approach to a difficult diagnostic problem]. Ned Tijdschr Geneeskd 1995 2.03
4 [A child with puzzling complaints--does he have a disease?]. Ned Tijdschr Geneeskd 1998 2.01
5 Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency. Proc Natl Acad Sci U S A 1987 1.98
6 Intestinal permeability in patients with coeliac disease and relatives of patients with coeliac disease. Gut 1993 1.79
7 Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome. Biochem Biophys Res Commun 1984 1.77
8 Effect of a new synbiotic mixture on atopic dermatitis in infants: a randomized-controlled trial. Clin Exp Allergy 2010 1.69
9 Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis. J Clin Invest 1988 1.68
10 The role of cisapride in the treatment of pediatric gastroesophageal reflux. The European Society of Paediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr 1999 1.56
11 Large daily fluctuations in plasma tyrosine in treated patients with phenylketonuria. Am J Clin Nutr 1996 1.47
12 [Fabry's disease; towards a treatment]. Ned Tijdschr Geneeskd 2000 1.45
13 [Measurement of selective intestinal permeability using a new, simple sugar absorption test]. Ned Tijdschr Geneeskd 1993 1.42
14 [Hypoglycemic ketoacidosis in children, a simple diagnosis with a simple therapy]. Ned Tijdschr Geneeskd 1994 1.39
15 Peroxisomal disorders in neurology. J Neurol Sci 1988 1.36
16 Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome). Nature 1983 1.35
17 Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome. Biochem Biophys Res Commun 1984 1.28
18 Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome. Biochem Biophys Res Commun 1985 1.28
19 Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatment. Hepatology 1994 1.28
20 Current concepts and issues in the management of regurgitation of infants: a reappraisal. Management guidelines from a working party. Acta Paediatr 1996 1.27
21 Repeatability of the sugar-absorption test, using lactulose and mannitol, for measuring intestinal permeability for sugars. J Pediatr Gastroenterol Nutr 1995 1.25
22 The daily gluten intake in relatives of patients with coeliac disease compared with that of the general Dutch population. Eur J Gastroenterol Hepatol 1997 1.22
23 Prognosis of extrahepatic biliary atresia. Arch Dis Child 1989 1.12
24 Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders. Biochem Biophys Res Commun 1988 1.08
25 Plasma phenylalanine and tyrosine responses to different nutritional conditions (fasting/postprandial) in patients with phenylketonuria: effect of sample timing. Pediatrics 1993 1.06
26 Rhizomelic chondrodysplasia punctata: another peroxisomal disorder. N Engl J Med 1985 1.05
27 Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literature. Eur J Pediatr 1997 1.04
28 Immortalized human hepatocytes as a tool for the study of hepatocytic (de-)differentiation. Cell Biol Toxicol 1997 1.04
29 Is encopresis always the result of constipation? Arch Dis Child 1994 1.01
30 Perinatal changes in myocardial metabolism in lambs. Circulation 2000 1.01
31 Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme. J Clin Invest 1990 1.01
32 [Quality of life in children with sickle cell disease in Amsterdam area]. Ned Tijdschr Geneeskd 1999 1.00
33 The inborn errors of peroxisomal beta-oxidation: a review. J Inherit Metab Dis 1990 1.00
34 Respiratory muscle activity in the assessment of bronchial responsiveness in asthmatic children. J Appl Physiol (1985) 1998 0.97
35 Clinical implications of the sugar absorption test: intestinal permeability test to assess mucosal barrier function. Scand J Gastroenterol Suppl 1997 0.97
36 Intestinal permeability in pediatric gastroenterology. Scand J Gastroenterol Suppl 1992 0.97
37 Physical adaptation of children to life at high altitude. Eur J Pediatr 1995 0.96
38 Age-related accumulation of phytanic acid in plasma from patients with the cerebro-hepato-renal (Zellweger) syndrome. Clin Chim Acta 1987 0.95
39 Catch-up growth in 60 children with celiac disease. J Pediatr Gastroenterol Nutr 1994 0.94
40 The cerebro-hepato-renal (Zellweger) syndrome. Impaired de novo biosynthesis of plasmalogens in cultured skin fibroblasts. Biochim Biophys Acta 1985 0.94
41 Gastrointestinal involvement in Langerhans' cell histiocytosis (Histiocytosis X): a clinical report of three cases. Eur J Pediatr 1990 0.94
42 Ultrastructure of the liver in th cerebrohepatorenal syndrome of Zellweger. Ultrastruct Pathol 1984 0.93
43 Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome. Eur J Pediatr 1984 0.93
44 Genetic relation between the Zellweger syndrome, infantile Refsum's disease, and rhizomelic chondrodysplasia punctata. N Engl J Med 1986 0.93
45 [Functional childhood gastrointestinal disorders. I. Chronic abdominal pain]. Ned Tijdschr Geneeskd 2003 0.91
46 [Functional childhood gastrointestinal disorders. III. Constipation and solitary encopresis; diagnostic work-up and therapy]. Ned Tijdschr Geneeskd 2003 0.91
47 Clinical recognition of patients affected by a peroxisomal disorder: a retrospective study in 40 patients. Eur J Pediatr 1992 0.90
48 Tyrosinaemia type I: considerations of treatment strategy and experiences with risk assessment, diet and transplantation. J Inherit Metab Dis 1995 0.90
49 [Chronic constipation in children; good results of biofeedback training as supplementary therapy]. Ned Tijdschr Geneeskd 1993 0.90
50 Phenylketonuria: plasma phenylalanine responses to different distributions of the daily phenylalanine allowance over the day. Pediatrics 1996 0.90
51 [Functional childhood gastrointestinal disorders. II. Constipation and solitary encopresis: physiology and pathophysiology]. Ned Tijdschr Geneeskd 2003 0.89
52 Tyrosinaemia type I: orthotopic liver transplantation as the only definitive answer to a metabolic as well as an oncological problem. J Inherit Metab Dis 1989 0.89
53 Intestinal permeability in exocrine pancreatic insufficiency due to cystic fibrosis or chronic pancreatitis. Pediatr Res 1996 0.88
54 Inspiratory stridor and dysphagia because of prolonged oesophageal foreign body. Eur J Pediatr 1987 0.88
55 Implementation of evidence-based practice: outside the box, throughout the hospital. Neth J Med 2011 0.87
56 Phenylketonuria. The in vivo hydroxylation rate of phenylalanine into tyrosine is decreased. J Clin Invest 1998 0.86
57 Follow-up of treated coeliac patients: sugar absorption test and intestinal biopsies compared. Eur J Gastroenterol Hepatol 1996 0.86
58 A milder variant of Zellweger syndrome. Eur J Pediatr 1985 0.85
59 Heterozygosity for the common LCHAD mutation (1528g>C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is low. Pediatr Res 2000 0.85
60 Nasogastric intubation as sole treatment of caustic esophageal lesions. Ann Otol Rhinol Laryngol 1985 0.84
61 Home care in cystic fibrosis patients. Eur Respir J 1995 0.83
62 Sensitivity of a hyperosmolar or "low"-osmolar test solution for sugar absorption in recognizing small intestinal mucosal damage in coeliac disease. Dig Liver Dis 2000 0.83
63 Perinatal changes in myocardial supply and flux of fatty acids, carbohydrates, and ketone bodies in lambs. Am J Physiol 1998 0.83
64 Prenatal and perinatal diagnosis of peroxisomal disorders. J Inherit Metab Dis 1989 0.82
65 A patient with lethal cardiomyopathy and a carnitine-acylcarnitine translocase deficiency. J Inherit Metab Dis 1995 0.82
66 Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndrome. J Lipid Res 1985 0.82
67 Coumarins during pregnancy: long-term effects on growth and development of school-age children. Thromb Haemost 2001 0.82
68 Should relatives of coeliacs with mild clinical complaints undergo a small-bowel biopsy despite negative serology? Eur J Gastroenterol Hepatol 2000 0.82
69 Severity scoring of atopic dermatitis: a comparison of three scoring systems. Allergy 1997 0.81
70 Vascular compromise prior to intestinal manifestations of Crohn's disease in a 14-year-old girl. J Pediatr Gastroenterol Nutr 1992 0.80
71 De novo malignancy after paediatric renal replacement therapy. Arch Dis Child 2001 0.80
72 Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies. Enzyme 1987 0.80
73 The cerebro-hepato-renal (Zellweger) syndrome: prenatal detection based on impaired biosynthesis of plasmalogens. Prenat Diagn 1986 0.80
74 Development of allergic disorders in children with cow's milk protein allergy or intolerance in infancy. Clin Exp Allergy 2000 0.80
75 Measurement of short-chain acyl-CoA dehydrogenase (SCAD) in cultured skin fibroblasts with hexanoyl-CoA as a competitive inhibitor to eliminate the contribution of medium-chain acyl-CoA dehydrogenase. Clin Chim Acta 1994 0.79
76 Intestinal carbamoyl phosphate synthase I in human and rat. Expression during development shows species differences and mosaic expression in duodenum of both species. J Histochem Cytochem 1998 0.79
77 Agreement between spirometry and tracheal auscultation in assessing bronchial responsiveness in asthmatic children. Respir Med 1999 0.78
78 Effect of disodiumcromoglycate on intestinal permeability changes and clinical response during cow's milk challenge. Pediatr Allergy Immunol 1993 0.78
79 Caustic esophageal lesions in childhood: prevention of stricture formation. J Pediatr Surg 1989 0.78
80 Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment. J Inherit Metab Dis 1987 0.77
81 Symptomatology and growth in infants with cow's milk protein intolerance using two different whey-protein hydrolysate based formulas in a Primary Health Care setting. Eur J Clin Nutr 1995 0.77
82 Age-related deficiency of the synthesis of platelet activating factor by leukocytes from Zellweger patients. Blood 1987 0.77
83 Age-related differences in plasmalogen content of erythrocytes from patients with the cerebro-hepato-renal (Zellweger) syndrome: implications for postnatal detection of the disease. J Inherit Metab Dis 1986 0.77
84 Use of tracheal auscultation for the assessment of bronchial responsiveness in asthmatic children. Thorax 1996 0.77
85 Myocardial lactate metabolism in fetal and newborn lambs. Circulation 1999 0.76
86 [One year of neonatal screening for sickle-cell disease in Emma Children's Hospital/Academic Medical Center in Amsterdam]. Ned Tijdschr Geneeskd 2001 0.76
87 A new, simple assay for long-chain acyl-CoA dehydrogenase in cultured skin fibroblasts using stable isotopes and GC-MS. Biochim Biophys Acta 1992 0.76
88 Nontransmural myocardial infarction as a complication of untreated cystic fibrosis. J Pediatr Gastroenterol Nutr 1990 0.76
89 A sibship with a mild variant of Zellweger syndrome. J Inherit Metab Dis 1987 0.75
90 [Qualitative malnutrition due to incorrect complementary feeding in Bush Negro children in Suriname]. Ned Tijdschr Geneeskd 2004 0.75
91 Pediatric duodenal biopsies: mucosal morphology and glycohydrolase expression do not change along the duodenum. J Pediatr Gastroenterol Nutr 1998 0.75
92 Diet and CO2-production in pediatric chronic pulmonary disease. J Pediatr Gastroenterol Nutr 1989 0.75
93 Platelet-activating factor: mediator of the third pathway of platelet aggregation? A study in three patients with deficient platelet-activating factor synthesis. J Clin Invest 1987 0.75
94 Child mortality and nutritional status of siblings. Lancet 1993 0.75
95 [The role of orthotopic liver transplantation in the treatment of metabolic diseases]. Ned Tijdschr Geneeskd 1992 0.75
96 The oto-palato-digital syndrome. J Laryngol Otol 1976 0.75
97 [Cystic fibrosis; pathophysiology of electrolyte transport and potential influence of amiloride]. Ned Tijdschr Geneeskd 1992 0.75
98 [Essential fatty acid deficiency in childhood]. Tijdschr Kindergeneeskd 1981 0.75
99 Behavioural outcome of school-age children after prenatal exposure to coumarins. Early Hum Dev 2000 0.75
100 [Standardized multidisciplinary diagnosis of cow's milk protein allergy in children. Work Group Cow's Milk Protein Allergy of the Groningen Academic Hospital]. Ned Tijdschr Geneeskd 1995 0.75
101 [Is circumoral cyanosis a sign of peripheral or of central cyanosis?]. Ned Tijdschr Geneeskd 1989 0.75
102 Polarizing inclusions in some organs of children with congenital peroxisomal diseases (Zellweger's, Refsum's, chondrodysplasia punctata (rhizomelic form), X-linked adrenoleukodystrophy). J Inherit Metab Dis 1988 0.75
103 [Immunology in medical practice. XXII. T-cells and strategies for tolerance induction]. Ned Tijdschr Geneeskd 1999 0.75
104 [Roentgen quiz. Ileo-ileal invagination in Henoch-Schoenlein disease]. Tijdschr Kindergeneeskd 1990 0.75
105 [Introduction of advanced medical equipment in the home situation]. Ned Tijdschr Geneeskd 1993 0.75
106 [Transient hyperphosphatasemia in infants and young children]. Tijdschr Kindergeneeskd 1986 0.75
107 [Limited value of routine preoperative laboratory studies in children]. Ned Tijdschr Geneeskd 1992 0.75
108 [Continuous intravenous antibiotic home treatment in 11 patients with cystic fibrosis in The Northern Netherlands]. Ned Tijdschr Geneeskd 1993 0.75
109 Increased paracellular macromolecular transport and subnormal glucose uptake in duodenal biopsies of patients with microvillus inclusion disease. Comparisons to other chronic diarrhea patients and to nondiarrhea patients. Ann N Y Acad Sci 2000 0.75
110 [Food as cause of atopic eczema in children]. Ned Tijdschr Geneeskd 1992 0.75
111 Cor pulmonale and acute liver necrosis, due to upper airway obstruction as part of pycnodysostosis. Eur J Pediatr 1984 0.75
112 [Cystic fibrosis and abdominal pain]. Ned Tijdschr Geneeskd 1988 0.75
113 [Treatment of acute liver insufficiency]. Ned Tijdschr Geneeskd 1980 0.75
114 The relation between gastro-oesophageal reflux, sleeping-position and sudden infant death and its impact on positional therapy. Eur J Pediatr 1997 0.75
115 Peroxisomal dysfunction in chondrodysplasia punctata, rhizomelic type. Ophthalmic Paediatr Genet 1987 0.75
116 Subnormal response of plasma glucose concentration to glucagon despite adequate glycogenolysis: the importance of kinetic measurements. Eur J Pediatr 2001 0.75
117 Catch-up growth following long-term administration of essential fatty acids in a girl with growth failure and essential fatty acid deficiency. Acta Paediatr Scand 1982 0.75
118 [Diagnosis of Zellweger's cerebrohepatorenal syndrome]. Tijdschr Kindergeneeskd 1984 0.75
119 [Medical education and scientific research: experiences with research training of Dutch students/physicians in the United States]. Ned Tijdschr Geneeskd 1994 0.75
120 Adenosine triphosphate-dependent copper transport in human liver. J Hepatol 1996 0.75
121 Deficient cholesterol side chain oxidation in patients without peroxisomes (Zellweger syndrome): evidence for the involvement of peroxisomes in bile acid synthesis in man. Clin Chim Acta 1987 0.75
122 Acyclovir for varicella in immunocompetent patients. Clin Investig 1993 0.75
123 Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease. J Neurol Sci 1988 0.75
124 [Diagnosis of celiac disease]. Ned Tijdschr Geneeskd 1987 0.75
125 Hepatic artery embolisation; successful treatment of multinodular haemangiomatosis of the liver. Eur J Pediatr 1986 0.75
126 [Zellweger syndrome and other peroxisomal disorders: II. (Bio)chemical characteristics of a recently discovered group of diseases]. Ned Tijdschr Geneeskd 1990 0.75
127 Prenatal detection of Zellweger syndrome. Lancet 1984 0.75
128 [Treatment of varicella with acyclovir in children with normal immune defense?]. Ned Tijdschr Geneeskd 1992 0.75
129 Prenatal diagnosis of the cerebro-hepato-renal (Zellweger) syndrome by detection of an impaired plasmalogen biosynthesis. J Inherit Metab Dis 1985 0.75
130 [X-linked adrenoleukodystrophy and other peroxisomal diseases caused by a failing peroxisomal beta-oxidation system: clinical expression, diagnosis and treatment]. Tijdschr Kindergeneeskd 1989 0.75
131 [A new biscuit free of cow's milk, chicken egg protein, lactose and gluten for children with food hypersensitivity]. Ned Tijdschr Geneeskd 1994 0.75
132 The value of the D-xylose test compared with the differential sugar absorption test in recognizing coeliac disease. Neth J Med 1996 0.75
133 [Meningism and meningitis, variations on a classical theme]. Ned Tijdschr Geneeskd 1989 0.75
134 [Swallowed foreign bodies in children]. Ned Tijdschr Geneeskd 1991 0.75
135 Regulation of lactase and sucrase-isomaltase gene expression in the duodenum during childhood. J Pediatr Gastroenterol Nutr 1998 0.75