John Dodge

John Dodge 's AcademicInfluence.com Rankings

John Dodge

Philosophy

#11385

World Rank

#15674

Historical Rank

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#8244

World Rank

#10286

Historical Rank

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Philosophy

Why Is John Dodge Influential?

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According to Wikipedia, John Ashton Dodge, CBE, FRCP, FRCPE, FRCPI, FRCPCH was a British paediatrician, specialising in cystic fibrosis. After his retirement in 1997, he became Emeritus Professor of Child Health at the Queen's University, Belfast, and Honorary Professor of Child Health at the University of Wales at Swansea.

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John Dodge 's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Randomised controlled trial of an aggressive nutritional regimen in sick very low birthweight infants (1997) (270)
Fibrosing colonopathy in cystic fibrosis: results of a case-control study (1995) (188)
Increased energy expenditure in cystic fibrosis is associated with specific mutations. (1992) (96)
Infantile hypertrophic pyloric stenosis in Belfast, 1957-1969. (1975) (83)
Indirect Pancreatic Function Tests in Children (2005) (80)
Oral-facial-digital syndrome. (1967) (63)
CUTIS GYRATUM, ACANTHOSIS NIGRICANS AND OTHER CONGENITAL ANOMALIES A NEW SYNDROME (1969) (61)
Production of Duodenal Ulcers and Hypertrophic Pyloric Stenosis by Administration of Pentagastrin to Pregnant and Newborn Dogs (1970) (60)
Congenital absence of islets of Langerhans. (1977) (59)
Rat small intestinal morphology and tissue regulatory peptides: effects of high dietary fat (1991) (58)
DEFECTIVE β-ADRENERGIC SECRETORY RESPONSES IN SUBMANDIBULAR ACINAR CELLS FROM CYSTIC FIBROSIS PATIENTS (1986) (58)
Cystic fibrosis-- current topics (1993) (57)
An international/multicentre report on patients with cystic fibrosis (CF) over the age of 40 years. (2008) (56)
The importance of rare diseases: from the gene to society (2010) (56)
Induction of pyloric hypertrophy by pentagastrin. An animal model for infantile hypertrophic pyloric stenosis. (1976) (51)
Shwachman–Diamond syndrome: UK perspective (2006) (50)
Nutritional Requirements in Cystic Fibrosis: A Review (1988) (48)
Cystic fibrosis: parents' response to the genetic basis of the disease. (1973) (48)
High-strength pancreatic enzyme supplements and large-bowel stricture in cystic fibrosis (1994) (47)
Nutrition and bronchopulmonary dysplasia. (1991) (47)
Effects of an artificial diet on growth of patients with cystic fibrosis. (1978) (44)
Diabetes mellitus in cystic fibrosis: a review. (1992) (39)
Huntington's chorea in children (1967) (34)
Letter: Essential fatty acid deficiency due to artificial diet in cystic fibrosis. (1975) (32)
Adrenergic secretory responses of submandibular tissues from control subjects and cystic fibrosis patients. (1985) (32)
Cystic fibrosis: nutritional consequences and management. (2006) (31)
Gene/energy interaction in cystic fibrosis (1990) (25)
Uptake of yeast (Saccharomyces boulardii) in normal and rotavirus treated intestine. (1996) (25)
Male fertility in cystic fibrosis (1995) (25)
Two cases of trisomy D associated with adrenal tumours. (1972) (23)
ABO blood groups and infantile hypertrophic pyloric stenosis. (1967) (23)
Effect of exercise on the nasal transmucosal potential difference in patients with cystic fibrosis and normal subjects. (1994) (23)
Paradoxical effects of essential fatty acid supplementation on lipid profiles and sweat electrolytes in cystic fibrosis (1990) (22)
Comparison between a standard pancreatic supplement and a high enzyme preparation in cystic fibrosis (1992) (21)
Energy intakes and losses in cystic fibrosis (1994) (20)
Psychosomatic aspects of infantile pyloric stenosis. (1972) (20)
Zinc deficiency syndrome in a British youth with cystic fibrosis. (1978) (19)
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency—diagnosis, plasma carnitine fractions and management in a further patient (1993) (19)
Defective beta-adrenergic secretory responses in submandibular acinar cells from cystic fibrosis patients. (1986) (18)
Psychological determinants of infantile pyloric stenosis. (1978) (17)
Stated Versus Actual Lipase Activity in Pancreatic Enzyme Supplements: Implications for Clinical Use (1995) (17)
De Lange's Amsterdam Dwarfs Syndrome A Case‐Report (1965) (17)
A millennial view of cystic fibrosis. (2015) (15)
Paediatric and Hereditary Aspects of Chronic Pancreatitis (1998) (15)
The Nutritional State and Nutrition (1985) (14)
IMPLICATIONS OF THE NEW GENETICS FOR SCREENING FOR CYSTIC FIBROSIS (1988) (14)
Cystic fibrosis serum stimulates mucin secretion but not calcium efflux from rat submandibular acini. (1983) (12)
Pancreatic enzyme supplements in cystic fibrosis (1991) (11)
Gastrointestinal tract and nutrition in cystic fibrosis: pathophysiology. (1986) (10)
Antiviral and antibacterial lipids in human milk and infant formula. (1991) (9)
EHLERS-DANLOS SYNDROME ASSOCIATED WITH ACQUIRED ENCEPHALOCELE. (1965) (9)
Surface features of small-intestinal mucosa in childhood diarrheal disorders. (1996) (9)
The aetiology of fibrosing colonopathy. (1996) (9)
Dietary management of cystic fibrosis. (1981) (9)
Abnormal distribution of ABO blood groups in infantile pyloric stenosis. (1971) (9)
Growth and milk intake of normal infants (2006) (9)
Experience with ceftazidime in cystic fibrosis. (1983) (8)
Pyloric stenosis and eosinophilic gastroenteritis in infants. (1988) (8)
Infantile Pyloric stenosis inheritance, psyche and soma (1973) (8)
Modulation of fluid absorption and the secretory response of rat jejunum to cholera toxin by dietary fat. (1990) (7)
Malnutrition and age-specific nutritional management in cystic fibrosis. (1992) (7)
Gluten intolerance, gluten enteropathy, and coeliac disease. (1980) (7)
Incidence of Molecular Forms of Bile Salt-Stimulated Lipase in Preterm and Term Human Milk (1998) (7)
Colonic strictures in cystic fibrosis. (1995) (7)
Further observations on a pedigree of the oral-facial-digital syndrome. (1969) (7)
Electronmicroscopy in 'absence' of islets of Langerhans in a newborn infant. (1982) (7)
Morphological aspects of particle translocation in vivo following ingestion of the yeast Saccharomyces boulardii. (1995) (7)
New possibilities for population control of cystic fibrosis. (1992) (6)
A complex biochemical modulation of intestinal ion transport in rats fed on high-fat diets. (1995) (6)
Further comments on fibrosing colonopathy study (2001) (5)
Adrenergic secretory responses of submandibular acinar cells from control subjects and cystic fibrosis patients (1985) (5)
Neonatal Infection Does Not Affect the Immunoreactive Trypsinogen Screening Test for Cystic Fibrosis (1994) (5)
Low butanol-extractable-iodine levels in the serum of patients with Down's syndrome. (1967) (5)
Kinetics of Viral Replication in Experimental Rotavirus Infection: Effects of High Dietary Fat (1991) (5)
Nutrition in cystic fibrosis: a historical overview (1992) (5)
Campylobacter Pylori and Reflux Oesophagitis (1990) (5)
Dietary fats and gastrointestinal function. (1994) (5)
Pancreatic enzyme therapy in cystic fibrosis (2008) (5)
Duodenal bile acids in diagnosis of congenital biliary atresia. (1983) (5)
Proceedings: Maternal factor in infantile hypertrophic pyloric stenosis. (1974) (4)
Pancreatic enzymes and Fibrosing Colonopathy. (2015) (4)
Exudate variation in the rabbit gastrointestinal tract: a scanning electron microscope study. (1990) (4)
Determinants of pancreatic and pulmonary status of cystic fibrosis (1991) (3)
Fatty acid composition of erythrocyte and small intestinal microvillus membranes: effects of high dietary fat (1992) (3)
Screening for cystic fibrosis: Why, how, and when? (1991) (3)
Fatty acids in cystic fibrosis in response to a marathon race. (1988) (3)
Familial Craniosynostosis with Oral Anomalies (1970) (3)
Comparison of three regimens in the management of acute gastroenteritis in infants (1990) (2)
Gene therapy for cystic fibrosis (1995) (2)
TOTAL ENERGY EXPENDITURE (TEE) IN EXTRAHEPATIC BILIARY ATRESIA (EHBA) (1991) (2)
Letter: Heterozygote advantage in cystic fibrosis. (1975) (2)
DOES DIETARY FAT AFFECT THE SEVERITY OF CHILDHOOD DIARRHOEA? (1989) (2)
Induction ofpyloric hypertrophy bypentagastrin Ananimal modelforinfantile hypertrophic pyloric stenosis (1976) (2)
SHORT STATURE AND MALNUTRITION IN CYSTIC FIBROSIS (1989) (2)
Nutritional aspects in cystic fibrosis. (1996) (2)
Fibrosing colonopathy: recent advances. (1996) (2)
Factors associated with chronic lung disease in preterm infants. (1992) (2)
Prostaglandins and cystic fibrosis. (1979) (2)
Study of breast feeding and hypertrophic pyloric stenosis does not conflict with others (1996) (2)
HETEROZYGOTE ADVANTAGE IN CYSTIC FIBROSIS (1975) (2)
Essential Fatty Acids, Prostaglandins and the Gastrointestinal Tract (1985) (1)
Proceedings: Absence of islets of Langerhans in pancreas of a newborn. (1975) (1)
Effects ofanartificial diet on growth ofpatients with cystic fibrosis (1978) (1)
Drs Evans and Dodge comment (1978) (1)
ERYTHROCYTE MEMBRANE FATTY ACID PROFILE IN CHINESE CHILDREN (1994) (1)
Height and weight in cystic ﬁbrosis: a cross sectional study (1998) (1)
MIXED MCT/LCT LIPID EMULSION USE IN SICK VLBW INFANTS (1994) (1)
Dr. Dodge comments as follows (1975) (1)
Gastro‐oesophageal reflux in infants (1999) (1)
Letter: Changing incidence of congenital pyloric stenosis. (1974) (1)
NEONATAL SCREENING FOR CYSTIC FIBROSIS (1986) (1)
THE EFFECTS OF SATURATED AND UNSATURATED FREE FATTY ACIDS ON CHLORIDE TRANSPORT IN RAT INTESTINE (1991) (0)
Ventilatory Equivalent for Oxygen before and during Exercise in 11 Cystic Fibrosis Patients with Mildly Reduced Pulmonary Function (1989) (0)
Patient-centred cystic fibrosis services. (2005) (0)
63 MODULATION OF THE SECRETORY RESPONSE TO CHOLERA TOXIN BY DIETARY FAT (1988) (0)
Gastrin Somatostatin and Infantile Pyloric Stenosis (1998) (0)
Symposium on 'Cystic Fibrosis' (1992) (0)
Liver Disorders in Childhood (1979) (0)
RESEARCH ON INFANTS (1977) (0)
Dietary fat in cystic fibrosis. (1994) (0)
Cystic Fibrosis (2020) (0)
Points from Letters: Essential Fatty Acid Deficiency Due to Artificial Diet in Cystic Fibrosis (1975) (0)
The Liver and Bilary System in Infants and Children (1980) (0)
Dr. J. Dodge and co-workers comment (1978) (0)
With commentary (1980) (0)
High-strength pancreatic enzyme supplements and large-bowel stricture in cystic fibrosis. (1994) (0)
Oral-facial-digi tal Syndrome (2011) (0)
Dr Dodge comments (1980) (0)
PYCNODYSOSTOSIS (1969) (0)
Confusion surrounding nitric oxide synthase/NADPH-diaphorase. (1996) (0)
Provision of Health Care for Cystic Fibrosis (1987) (0)
Infantile hypertrophic pyloric stenosis. (1977) (0)
Neonatal pyloric hypertrophy and duodenal ulceration produced by pentagastrin. (1969) (0)
infants nutritional regimen in sick very low birthweight Randomised controlled trial of an aggressive and (1998) (0)
Cystic Fibrosis Pulmonary Infections: The UK Experience (1996) (0)
WS09.6 Telomere length in cystic fibrosis patients – are patients with CF ageing too quickly? (2017) (0)
GENOTYPE IDENTIFICATION CHARACTERISED BY VARIATION IN BASAL METABOLIC RATE IN CYSTIC FIBROSIS (1991) (0)
OFD syndrome. (1970) (0)
Abnormal Distribution ofABOBlood Groups inInfantile Pyloric Stenosis (1971) (0)
Molecular Forms of Bile Salt Stimulated Lipase in Human Milk (1997) (0)
fibrosis . growth of patients with cystic Effects of an artificial diet on (0)
The effects of high fat diet on ionic transport in rat intestine. (1991) (0)
Commentary (1991) (0)
Gene therapy for cystic fibrosis: what message for the recipient? (1998) (0)

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What Schools Are Affiliated With John Dodge ?

John Dodge is affiliated with the following schools:

Queen's University Belfast