Search

Your search keyword '"CAHALANE, S. F."' showing total 113 results
Start Over Author "CAHALANE, S. F."
113 results on '"CAHALANE, S. F."'

3. Irish Paediatric Association Annual Clinical Meeting, Limerick, May 15th–16th, 1987

Author

Dykes, Evelyn, O’Donnell, Barry, Leahy, F., Hendow, H., Matthews, T. G., Clarke, T. A., Connolly, B., Guiney, E. J., Kneafsey, P., Kelehan, P., McKay, M., Hensey, O., Curtis, P., Matthews, T., Crowley, P., Griffin, E., O’Connell, P., Gorman, W., O’Brien, N., O’Herlihy, C., Clarke, T., Darling, M., O’Regan, M., Hynes, D., McManus, F., Maguire, Sabine, Moriarty, Patricia, Tempany, E., Fitzgerald, M., Murphy, Colleen, Connolly, K., Koura, I., Cosgrove, J. F., Lillis, D. F., Fitzgerald, R. J., Dunne, K., Geary, D. F., Ikse, K. -Haka, Seckert, D., Coulter, P., Quinn, C. M., Kelly, D. G., Cahalane, S. F., Moore, D. P., O’Meara, A., Breathnach, F., Rollins, M. D., Shields, M. D., Quinn, R. J. M., Wooldridge, M. A., Hoey, Hilary, Colaco, J., Egan-Mitchell, B., Stevens, F. M., Fottrell, P. F., McCarthy, C. F., McNicholl, B., Corcoran, B., Healy, R., Mian, M., Henvill, D., Piggott, E., Corboy, A., Keating, J. F., Regan, P., King, M., O’Donnabhain, D., Duff, D. F., McMenamin, J., Gorman, W. A., and Denham, B.

Published
1988
Full Text
View/download PDF

5. Book reviews

Author

Mowbray, John, Gatenby, P. B. B., O’Malley, Eoin, Masterson, Joseph, Cantwell, D. F., Cahalane, S. F., Nelson, H. G., Mowbray, John, McKeever, J. D., Meenan, F. O., O’Meara, R. A. Q., Joyce, Patrick Dwyer, Mellon, Douglas E., Lyons, J. B., Kernan, R. P., Smyth, A., O’Halloran, M. J., Roe, Peter F., Chevasse, Judith M., O’Dwyer, W. F., Mellon, D. E., Breathnach, C. S., S.K., Lyons, J. B., Lyons, J. B., Thompson, Alan, and Kennedy, Desmond

Published
1968
Full Text
View/download PDF

7. Book reviews

Author

Coakley, J. B., Kernan, R. P., Fitzgerald, Oliver, Jessop, W. J. E., Gregg, Thomas M., Nelson, H. G., Henderson, H. J. R., Walsh, Anthony, Walsh, Anthony, O’Brien, Brendan, Walsh, Anthony, Doyle-Kelly, W., Bourke, Geoffrey J., Mulcahy, Risteard, Cross, Finbarr H., Baxter, J. T., Byrnes, C. K., Boggust, W. A., Boggust, W. A., Brady, Gerard, Cahalane, S. F., Ryan, Max, Kebnan, Roderick P., Nelson, H. G., Fenelon, Eric, Timoney, F. J., Moriarty, M. A., and McCollum, Stanley T.

Published
1965
Full Text
View/download PDF

8. Book reviews

Author

McGrath, S. Desmond, Steen, R. E., Somerville-Large, L. B., McAuley, F. D., Cahalane, S. F., Ryder, R. J. W., Shaw, K. M., Bourke, Geoffrey J., Doyle-Kelly, W., Walsh, M. M., Douglas, SHOLTO, Kane, FRANK, Murnaghan, M. F., Roe, P. F., Henry, F. J., TEMPERLEY, I. J., O’regan, John B., Healy, J. B., and Somerville-large, L. B.

Published
1965
Full Text
View/download PDF

10. Book reviews

Author

Lyons, J. B., Devlin, James G., O’Toole, P., O’B. Hourihane, D., Lanigan, J. P., Bourke, Geoffrey J., Kernan, R. P., Keaveny, T. V., Cahalane, S. F., and Towers, Robert P.

Published
1973
Full Text
View/download PDF

11. Book reviews

Author

O’Meara, R. A. Q., Ryan, Max J., Cahalane, S. F., Erskine, C. A., Doyle, Eric E., Bourke, Geoffrey J., Kane, Frank, and Malone, John P.

Published
1967
Full Text
View/download PDF

12. Book reviews

Author

Hingerty, D., Somerville-Large, L. B., Mulcahy, R., Daly, H. W., Roche, T. F., Micks, R. H., Henry, F. J., Kernan, R. P., Holland, P. D. J., Donovan, D. E., Weir, D. G., Devlin, J., O'Donovan, D. K., Cahalane, S. F., Pringle, Brian, Moriarty, M. A., O'Morchoe, C. C. C., Cherry, J. C., Roe, P. F., O'Shea, Michael J., Steen, R. E., Verling, W. H., and Lyons, J. B.

Published
1965
Full Text
View/download PDF

13. Book reviews

Author

Holmes, W. J., O’Brien, Catherine, Kelly, W. Doyle, Curtin, Muriel F., Malone, John P., Mulcahy, Ristead, MacDonald, A. J., Browne, Harold, Moorhouse, Ellen C., McCarthy, John R., Mehigan, J. A., Lyons, J. B., Erskine, C. A., Lyons, J. B., Boland, S. J., Clery, Anthony P., Cahalane, S. F., O’Connell, N. D., Breathnach, C. S., O’Halloran, M. J., Mullaney, Joan, Henderson, H. J. R., Walsh, Joseph, Kane, F., Ward, Conor, and Guinan, P. M.

Published
1968
Full Text
View/download PDF

14. Book reviews

Author

Moonhouse, Ellen C., Mellon, Douglas E., Keogh, Roma, Breathnach, C. S., Bourke, Geoffrey J., Cahalane, S. F., Shaw, K. M., Chambers, P. L., Chambers, C. M., Malone, J. P., Mitchell, David, Tomkin, A., Curtin, Flavien, Meenan, F. O. C., Rees, J. P. R., and Martin, E. A.

Published
1971
Full Text
View/download PDF

15. Book reviews

Author

Steen, R. E., Cantwell, D. F., Cahalane, S. F., Wilson, Robert, Barniville, H. T., Linehan, W. D., Kernan, R. P., Conalty, M. L., Kirker, J. G., Kernan, R. P., Clery, A. B., Curtin, J. McAuliffe, Drury, M. I., Jaswon, N., Brady, Gerard, Mowbray, John, Tempany, Edward, Breathnach, C. S., Baker, R. S. W., Quinn, Catherine, Cantwell, D. F., O’Donovan, D. K., Browne, Harold J., Shaw, Keith M., Gatenby, P. B. B., O’Connor, J. E., Cherry, J. C., Hewson, G. Everard, Lane, David, Mullaney, Joan, and de Lourdes, M.

Published
1968
Full Text
View/download PDF

17. Book reviews

Author

Breathnach, C. S., Cahalane, S. F., Erskine, C. A., Lyons, J. B., Ryan, Max J., Kebnan, B. P., Drury, M. I., and Browne, Patrick A.

Published
1966
Full Text
View/download PDF

18. Book reviews

Author

Powell, David, Feeney, J. K., Fleetwood, J., Linehan, W. D., Breathnach, C. S., Stevens, Patricia F., Hourihane, D. O’B., Lyons, J. B., Buckley, M. P., Macauley, PATRICK, Cahalane, S. F., and Martin, EDWARD A.

Published
1971
Full Text
View/download PDF

19. Section of biological sciences: Proceedings of the meeting at University College, Dublin on July 3rd and 4lh, 1972.

Author

Mullins, Catherine, Cahalane, S. F., Harrington, M. G., Skelly, Jacintha M., Brennan, P. J., Blair, Carol D., Gaffney, P. J., Ryan, J. Philip, Duke, Eamon J., O’Donnell, D., McGeeney, K. F., FitzGerald, M. J. T., Cunningham, R. M., Folan, J. C., Little, C. L. M., O’Brien, T. M., Bridges, J. B., Keenan, D. J. M., McHale, N., Roddie, I. C., Bamford, D. R., Jeal, F., West, A. B., McCarthy, Ina, Kernan, R. P., Murphy, P. J., Sheehan, J. D., Hall, W. J., Martin, J. D. G., Hall, W. J., O’Regan, M. G., Kirkpatrick, C. T., MacLaren, A., Pollock, D., Abram, W. P., Allen, J. A, Roddie, I. C., O’Malley, K., Stevenson, I. H., Canon, Paul J., Hart, Nora F., Kumar, S., Bridges, J. B., Surgeon, I. C., Wallace, W. F. M., Hobbs, Frances M., Surgeon, I. C., Wallace, W. F. M., Gowing, W. H., Roddie, I. C., Kingston, T. P., O’Connor, P. C., and Slater, P.

Published
1973
Full Text
View/download PDF

21. Book reviews

Author

Cahalane, S. F., Muldowney, F. P., Kirwan, Wm. O., Martin, E. A., O’Doherty, Neil, Moloney, Michael, Murphy, M. K., Towers, Robert P., Mitchell, D. M., and Solomons, Michael

Published
1976
Full Text
View/download PDF

25. Book reviews

Author

Cahalane, S. F., Joyce, Patrick Dwyer, Hingerty, D., Hogan, David, Breathnach, C. S., Timoney, F. J., and McNulty, James G.

Published
1970
Full Text
View/download PDF

26. Book reviews

Author

Coakley, J. B., Cahalane, S. F., Kennedy, George F., Kirker, J. G., Weir, D. G., and McCabe, A. M. E.

Published
1962
Full Text
View/download PDF

29. Spontaneous Resolution of Histiocytosis X: Report of a Case

Author

Meenan, F. O. and Cahalane, S. F.

Abstract

A case of histiocytosis X with spontaneous remission is described. The patient presented is an infant of six months, with cutaneous and bony lesions. No specific treatment was given, but the child was free of signs and symptoms two years later. The histological findings of eosinophils and fibrosis are probably of good prognostic import.

Published
1967
Full Text
View/download PDF

31. Renal Dysplasia-a Clnicopathologcal Review.

Author

QUINN, CECILY M., KELLY, D. G., and CAHALANE, S. F.

Abstract

- A review of 15 cases of unilateral renal dysplasia is presented. Seven patients came to medical attention with urinary tract infection. Only 4 presented with an abdominal mass. Eight patients were found to have ipsilateral ureteric anomalies and 4 of these also had contralateral ureteric problems. Five patients had extra-renal anomalies and these included Turner's syndrome, scoliosis and congenital dislocation of the hip. Histological examination, in all cases, revealed the presence of primitive ducts surrounded by concentric layers of cellular mesenchyme. Metaplastic cartilage was noted in only 7 of the 15 cases. [ABSTRACT FROM AUTHOR]

Published
1988
Full Text
View/download PDF

33. BULLOUS PEMPHIGOID OF CHILDHOOD AND COELIAC DISEASE.

Author

F. O. C. Meenan and Cahalane, S. F.

Subjects
DISEASES, CHILDREN, CELIAC disease, CASE studies, PATIENTS, DIGESTIVE system diseases
Abstract

The case of a boy aged 3 with bullous pemphigoid, who also had clinical and pathological evidence of coeliac disease, is described. Two brothers had coeliac disease. The association of the 2 conditions is interesting but it is not suggested on the present evidence that there is a causal relationship between them. [ABSTRACT FROM AUTHOR]

Published
1969
Full Text
View/download PDF

43. Galactosaemia--a controversial disorder. Screening & outcome. Ireland 1972-1992.

Author

Badawi N, Cahalane SF, McDonald M, Mulhair P, Begi B, O'Donohue A, and Naughten E

Subjects
Adolescent, Adult, Child, Child, Preschool, Galactosemias mortality, Galactosemias physiopathology, Galactosemias prevention & control, Humans, Incidence, Infant, Infant, Newborn, Ireland epidemiology, Prognosis, Sampling Studies, Survival Rate, Galactosemias epidemiology, Mass Screening
Abstract

We reviewed 20 years (from 1972 to 1992) of screening for galactosaemia in Ireland. We looked at a small group of 32 patients followed up in the same centre since diagnosis. 1.2 million babies have been screened with 55 cases of classical galactosaemia and 7 Duarte Variants being detected. The frequency is thus, 1:23,000 and is increased among itinerants to 1:700. The mean age of diagnosis was 6.9 days with 41/62 cases symptomatic at the time. There were 9 deaths, 8 in the first 10 years, six of whom were itinerants. On follow up of the 32 children, who have attended Temple Street Hospital, 13/32 have no detectable complication. Nineteen show either one or a combination of cataracts, speech problems, tremors, abnormal FSH and or LH, delayed mental development and recurring infections. The screening test is the Bacterial Inhibition Assay with Beutler test, an original blood spot as confirmation in presumptive possible cases. The Beutler test is performed urgently in high risk situations. Five classical galactosaemics gave false negative results, 3 because of poor feeding, and two because of soya milk formulas. Screening prevented deaths as 7/84 siblings of our cases were unexpected infant deaths, all but one predating screening. Unexplained delay in screening undermines its effectiveness. Survival is enhanced by aggressive neonatal care. Symptoms are improved on commencing diet, with cataracts regressing. Complications did not correlate with the day of starting diet. Galactose-1-Phosphate and urinary galactitol levels did not correlate with complications, but slit lamp examination has proved a helpful index of adherence to diet. The mechanism of complications is unclear, and it is essential that current research should be aggressively pursued to explain mental deficiency in cases treated either pre-natally or early in post natal life.

Published
1996

44. Molecular analysis of PKU in Ireland.

Author

O'Neill CA, Eisensmith RC, Croke DT, Naughten ER, Cahalane SF, and Woo SL

Subjects
Haplotypes, Humans, Ireland epidemiology, Polymorphism, Restriction Fragment Length, Prevalence, Gene Frequency, Minisatellite Repeats genetics, Mutation genetics, Phenylketonurias epidemiology, Phenylketonurias genetics
Abstract

Classical phenylketonuria (PKU: McKusick No. 261600) is caused by mutations occurring at the phenylalanine hydroxylase (PAH) locus on chromosome 12 and has a prevalence in Ireland of 1 in 4500. We examined 304 independent alleles from 350 patients for the presence of six mutations and have characterized VNTR alleles within the minisatellite region 3' to the PAH gene in patients carrying the most prevalent mutation. R408W was the most common mutation found, with a relative frequency of 42%. All other mutations had relative frequencies of < 10%. VNTR analysis showed that the R408W mutation is associated with the VNTR-8 allele in the Irish population, indicating that R408W is associated with RFLP haplotype 1. This differs from that reported from eastern Europe where R408W is associated with RFLP haplotype 2/VNTR-3; an observation which has led several groups to propose a Balto-Slavic origin for this mutation. These results support the hypothesis of a second, independent founding event for the R408W mutation on an RFLP haplotype 1 VNTR-8 chromosome background in the Irish/Celtic population.

Published
1994
Full Text
View/download PDF

46. Birth weight and pathogenesis in phenylketonuria.

Author

Crockett DJ, Woolf LI, McBean MS, Woolf FM, and Cahalane SF

Subjects
Humans, Infant, Newborn, Phenylketonurias etiology, Phenylketonurias genetics, Reference Values, Birth Weight, Phenylketonurias pathology
Abstract

The birthweights of an ethnically homogeneous sample of infants with phenylketonuria, their unaffected siblings, and control infants were compared after adjusting for the effects of: mother's age, mother's date of birth, mother's height and obstetric history, the length of gestation, the infant's sex, the place and date of birth. There were no significant differences between the infants with phenylketonuria and their unaffected siblings either in adjusted or unadjusted birthweights. Control infants had slightly, but statistically significant, greater adjusted and unadjusted birthweights than the combined phenylketonuria and unaffected sibling groups. This effect of the phenylketonuria gene is a previously unreported finding but unlikely to be related to the pathogenesis of phenylketonuria. Our results do not provide support for the "justification" hypothesis that the mental and neurological defects in phenylketonuria result from prenatal tyrosine deprivation which would be reflected in lower birthweights.

Published
1990
Full Text
View/download PDF

47. Malignant rhabdoid tumour of soft tissue. An ultrastructural and immunohistological study of a pelvic tumour.

Author

Dervan PA, Cahalane SF, Kneafsey P, Mynes A, and McAllister K

Subjects
Child, Diagnosis, Differential, Female, Humans, Microscopy, Electron, Pelvic Neoplasms analysis, Rhabdomyosarcoma analysis, Soft Tissue Neoplasms analysis, Vimentin analysis, Pelvic Neoplasms ultrastructure, Rhabdomyosarcoma ultrastructure, Soft Tissue Neoplasms ultrastructure
Abstract

A case of extrarenal malignant rhabdoid sarcoma arising in the pelvic soft tissues of a 12-year-old girl is described. By routine light microscopy the tumour resembled, in some areas, an embryonal rhabdomyosarcoma and, in other areas, a neuroblastoma. Electron microscopy revealed characteristic cytoplasmic aggregates of intermediate filaments, often with central clusters of organelle membranes surrounded by these filaments. Immunohistochemical stains showed strong cytoplasmic reactivity for vimentin. Staining for cytokeratin, myoglobin, desmin, neurofilaments, neurone specific enolase, S-100 protein and leucocyte common antigen was negative. A histogenetic origin from primitive mesenchymal cells is favoured. We strongly support the use of electron microscopy for the definitive diagnosis of small round cell undifferentiated sarcomas of childhood.

Published
1987
Full Text
View/download PDF

48. Schizophrenia and coeliac disease.

Author

Dean G, Hanniffy L, Stevens F, Temperley I, O'Broin JD, Scott J, and Cahalane SF

Subjects
Biopsy, Celiac Disease blood, Celiac Disease epidemiology, Female, Folic Acid Deficiency etiology, Humans, Intestines pathology, Male, United Kingdom, Celiac Disease complications, Folic Acid blood, Schizophrenia complications
Published
1975

49. Fulminant meningococcal septicaemia. A hospital experience.

Author

Cahalane SF and Waters M

Subjects
Autopsy, Child, Child, Preschool, Female, Heparin therapeutic use, Hospitals, Pediatric, Humans, Hydrocortisone therapeutic use, Infant, Ireland, Male, Meningococcal Infections microbiology, Meningococcal Infections pathology, Neisseria meningitidis isolation & purification, Penicillins therapeutic use, Seasons, Sepsis microbiology, Sepsis pathology, Serotyping, Social Class, Sulfonamides therapeutic use, Meningococcal Infections diagnosis, Sepsis diagnosis
Abstract

In the first 5 months of 1975, 12 cases of meningococcal septicaemia were seen at a children's hospital where in previous years the condition was seen only sporadically. 3 of these children were dead on admission, 5 died shortly after admission, and 4 responded to treatment. Neisseria meningitidis was recovered from cerebrospinal fluid or blood or both in all cases, and the clinical illness was characterised by fever, prostration, and cutaneous purpura of abrupt onset. There were no significant previous illnesses, no recognisable prodromata, and, bacteriology apart, no pattern of laboratory results. There was a suggestion of centre-city clustering in the home background, although 2 of the patients came from rural areas. At necropsy gross adrenal haemorrhage was found in 6 of the 8 fatal cases, and upper gastrointestinal bleeds in the 5 deaths which were not sudden.

Published
1975
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results