Literature DB >> 1345103

Bone marrow transplants in genetic diseases.

J R Hobbs1.   

Abstract

The first paper [9] advocating the displacement use of bone marrow transplantation (DBMT) to treat a variety of genetic metabolic diseases (including thalassaemia major) was put before a European Working Party in 1978. It evolved from mainly Westminster experience which showed the need [6] for DBMT and first successfully used donors other than matched siblings [9]. The principles of using DBMT to install a donor marrow as a component factory which can last a lifetime are outlined. It is not a panacea, being applicable to only about 7% of known inborn errors. Worthwhile correction of some 50 previously disabling diseases in over 700 patients has already been achieved worldwide and for most of the survivors no further treatment is used after 1 year. Guidelines for future extension, including gene transplants, are offered. The superior results of elective DBMT (about 95%) should encourage paediatricians to aim for earlier diagnoses and evaluations for transplants.

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Year:  1992        PMID: 1345103     DOI: 10.1007/bf02125802

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  25 in total

1.  Who pioneered the use of alternative donors (and stem cells from peripheral blood) in bone marrow transplantation?

Authors:  K Hughes-Jones; S Selwyn; P G Riches
Journal:  Arch Dis Child       Date:  1991-09       Impact factor: 3.791

Review 2.  Displacement bone marrow transplantation and immunoprophylaxis for genetic diseases.

Authors:  J R Hobbs
Journal:  Adv Intern Med       Date:  1988

3.  Treatment of metachromatic leukodystrophy in fibroblasts by enzyme replacement.

Authors:  U N Wiesmann; E E Rossi; N N Herschkowitz
Journal:  N Engl J Med       Date:  1971-03-25       Impact factor: 91.245

4.  Bone marrow transplantation for inborn errors.

Authors:  J R Hobbs
Journal:  Lancet       Date:  1981-10-03       Impact factor: 79.321

5.  Experience with bone marrow transplantation for inborn errors of metabolism.

Authors:  J R Hobbs
Journal:  Enzyme       Date:  1987

6.  Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease.

Authors:  N W Barton; R O Brady; J M Dambrosia; A M Di Bisceglie; S H Doppelt; S C Hill; H J Mankin; G J Murray; R I Parker; C E Argoff
Journal:  N Engl J Med       Date:  1991-05-23       Impact factor: 91.245

7.  Bone marrow transplantation in canine mucopolysaccharidosis I. Effects within the central nervous system.

Authors:  R M Shull; N E Hastings; R R Selcer; J B Jones; J R Smith; W C Cullen; G Constantopoulos
Journal:  J Clin Invest       Date:  1987-02       Impact factor: 14.808

8.  Bone marrow transplantation for sickle cell disease. A study of parents' decisions.

Authors:  E Kodish; J Lantos; C Stocking; P A Singer; M Siegler; F L Johnson
Journal:  N Engl J Med       Date:  1991-11-07       Impact factor: 91.245

9.  Correction of abnormal cerebroside sulfate metabolism in cultured metachromatic leukodystrophy fibroblasts.

Authors:  M T Porter; A L Fluharty; H Kihara
Journal:  Science       Date:  1971-06-18       Impact factor: 47.728

Review 10.  Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics.

Authors:  J F Kerr; A H Wyllie; A R Currie
Journal:  Br J Cancer       Date:  1972-08       Impact factor: 7.640

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  2 in total

Review 1.  Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparison.

Authors:  E Treacy; B Childs; C R Scriver
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

2.  Stem Cell Applications in Lysosomal Storage Disorders: Progress and Ongoing Challenges.

Authors:  Sevil Köse; Fatima Aerts-Kaya; Duygu Uçkan Çetinkaya; Petek Korkusuz
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

  2 in total

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