Literature DB >> 846387

Cystic fibrosis: a new outlook. 70 patients above 25 years of age.

H Shwachman, M Kowalski, K T Khaw.   

Abstract

We have presented a group of 70 patients over 25 years of age as of January 1, 1975, who were diagnosed as having cystic fibrosis (CF) at various ages from birth to 28 years. Some patients were diagnosed late in life in spite of classical symptoms and a characteristic history of the disease. Patients with CF present with a broad spectrum of symptoms which vary considerably in severity. This older age group represents approximately 10% of our current roster of patients with CF. This disease is no longer confined to early life and will continue to be seen with increasing frequency in older patients. Our experience with this disease indicates that a number of affected individuals can attain adulthood and find a useful place in society. The quality of life provided to these adults is illustrated in their intellectual, socioeconomic achievements and marital life. Our aim has been to recognize the disease as early in life as possible and to provide a comprehensive medical program which includes all aspects of health care.

Entities:  

Mesh:

Substances:

Year:  1977        PMID: 846387

Source DB:  PubMed          Journal:  Medicine (Baltimore)        ISSN: 0025-7974            Impact factor:   1.889


  24 in total

1.  Glucose tolerance in cystic fibrosis.

Authors:  S Lanng; B Thorsteinsson; G Erichsen; J Nerup; C Koch
Journal:  Arch Dis Child       Date:  1991-05       Impact factor: 3.791

Review 2.  Pathogenesis and management of arthropathy in cystic fibrosis.

Authors:  B M Phillips; T J David
Journal:  J R Soc Med       Date:  1986       Impact factor: 5.344

Review 3.  [Diseases of the paranasal sinuses and their relation to respiratory tract diseases].

Authors:  H G Wiesemann; U Stephan
Journal:  Arch Otorhinolaryngol       Date:  1982

4.  The pathology of meconium ileus equivalent.

Authors:  I Jeffrey; D Durrans; M Wells; H Fox
Journal:  J Clin Pathol       Date:  1983-11       Impact factor: 3.411

5.  Hypertrophic pulmonary osteoarthropathy in cystic fibrosis.

Authors:  A M Crawford; H R Rabin; M J Fritzler
Journal:  Rheumatol Int       Date:  1985       Impact factor: 2.631

6.  An approach for treating the hepatobiliary disease of cystic fibrosis by somatic gene transfer.

Authors:  Y Yang; S E Raper; J A Cohn; J F Engelhardt; J M Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-15       Impact factor: 11.205

7.  Talc poudrage in the treatment of spontaneous pneumothoraces in patients with cystic fibrosis.

Authors:  C G Tribble; R F Selden; B M Rodgers
Journal:  Ann Surg       Date:  1986-12       Impact factor: 12.969

8.  Spontaneous bacterial peritonitis in cystic fibrosis.

Authors:  C F Doershuk; R C Stern
Journal:  Gut       Date:  1994-05       Impact factor: 23.059

9.  Pancreatitis as initial presentation of cystic fibrosis in young adults. A report of two cases.

Authors:  T J Masaryk; E Achkar
Journal:  Dig Dis Sci       Date:  1983-10       Impact factor: 3.199

10.  Respiratory tract disease and obstructive azoospermia.

Authors:  E Neville; R Brewis; W K Yeates; A Burridge
Journal:  Thorax       Date:  1983-12       Impact factor: 9.139

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.