Literature DB >> 8223821

Elevation of transaminases as an early sign of late-onset glycogenosis type II.

M T Di Fiore, R Manfredi, L Marri, A Zucchini, L Azzaroli, G Manfredi.   

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Year:  1993        PMID： 8223821     DOI： 10.1007/bf01954008

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


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  9 in total

1.  Acid maltase deficiency: a case study and review of the pathophysiological changes and proposed therapeutic measures.

Authors:  H Isaacs; N Savage; M Badenhorst; T Whistler
Journal:  J Neurol Neurosurg Psychiatry       Date:  1986-09       Impact factor: 10.154

2.  [Clinical follow-up in the adult (myopathic) form of glycogenosis type II].

Authors:  P Schejbal; M Kutzner; H W Delank; F Gullotta
Journal:  Schweiz Arch Neurol Psychiatr (1985)       Date:  1986

3.  Juvenile-onset acid maltase deficiency with unusual familial features.

Authors:  M J Danon; S DiMauro; S Shanske; F L Archer; A F Miranda
Journal:  Neurology       Date:  1986-06       Impact factor: 9.910

4.  Persistent elevation of transaminases as the presenting finding in an adolescent with an unsuspected muscle glycogenosis.

Authors:  W R Treem
Journal:  Clin Pediatr (Phila)       Date:  1987-11       Impact factor: 1.168

5.  The spectrum and diagnosis of acid maltase deficiency.

Authors:  A G Engel; M R Gomez; M E Seybold; E H Lambert
Journal:  Neurology       Date:  1973-01       Impact factor: 9.910

6.  Protein turnover in acid maltase deficiency before and after treatment with a high protein diet.

Authors:  A M Umpleby; C M Wiles; P S Trend; I N Scobie; A F Macleod; G T Spencer; P H Sonksen
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-05       Impact factor: 10.154

7.  Acid maltase deficiency in adults. Diagnosis and management in five cases.

Authors:  P S Trend; C M Wiles; G T Spencer; J A Morgan-Hughes; B D Lake; A D Patrick
Journal:  Brain       Date:  1985-12       Impact factor: 13.501

8.  Childhood acid maltase deficiency. A clinical, biochemical, and morphologic study of three patients.

Authors:  T Matsuishi; M Yoshino; K Terasawa; I Nonaka
Journal:  Arch Neurol       Date:  1984-01

9.  A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studies.

Authors:  M C Loonen; H F Busch; J F Koster; J J Martin; M F Niermeijer; A W Schram; B Brouwer-Kelder; W Mekes; R G Slee; J M Tager
Journal:  Neurology       Date:  1981-10       Impact factor: 9.910
  9 in total
  2 in total

1.  Pompe disease diagnosis and management guideline.

Authors:  Priya S Kishnani; Robert D Steiner; Deeksha Bali; Kenneth Berger; Barry J Byrne; Laura E Case; Laura Case; John F Crowley; Steven Downs; R Rodney Howell; Richard M Kravitz; Joanne Mackey; Deborah Marsden; Anna Maria Martins; David S Millington; Marc Nicolino; Gwen O'Grady; Marc C Patterson; David M Rapoport; Alfred Slonim; Carolyn T Spencer; Cynthia J Tifft; Michael S Watson
Journal:  Genet Med       Date:  2006-05       Impact factor: 8.822

2.  Clinical Analysis of Algerian Patients with Pompe Disease.

Authors:  Y Sifi; M Medjroubi; R Froissart; N Taghane; K Sifi; A Benhabiles; S Lemai; S Semra; H Benmekhebi; Z Bouderda; N Abadi; A Hamri
Journal:  J Neurodegener Dis       Date:  2017-02-06
  2 in total

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