Literature DB >> 4502299

Glycogenosis. IV. A new cause of infantile hypotonia.

H Zellweger, S Mueller, V Ionasescu, S S Schochet, W F McCormick.   

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Year:  1972        PMID： 4502299     DOI： 10.1016/s0022-3476(72)80144-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  13 in total

1.  [Polyglycosan body myopathy].

Authors:  M Jeub; K Kappes-Horn; C Kornblum; D Fischer
Journal:  Nervenarzt       Date:  2006-12       Impact factor: 1.214

2.  Liver transplantation for type IV glycogen storage disease.

Authors:  R Selby; T E Starzl; E Yunis; B I Brown; R S Kendall; A Tzakis
Journal:  N Engl J Med       Date:  1991-01-03       Impact factor: 91.245

Review 3.  Cell migration and chimerism after whole-organ transplantation: the basis of graft acceptance.

Authors:  T E Starzl; A J Demetris; M Trucco; N Murase; C Ricordi; S Ildstad; H Ramos; S Todo; A Tzakis; J J Fung
Journal:  Hepatology       Date:  1993-06       Impact factor: 17.425

Review 4.  The glycogen storage diseases.

Authors:  B E Ryman
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

5.  Severe neonatal onset of glycogenosis type IV: clinical and laboratory findings leading to diagnosis in two siblings.

Authors:  B Giuffrè; R Parini; T Rizzuti; L Morandi; O P van Diggelen; C Bruno; M Giuffrè; G Corsello; F Mosca
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

6.  Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).

Authors:  J M Schröder; R May; Y S Shin; M Sigmund; S Nase-Hüppmeier
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

7.  Clinical and laboratory findings in four patients with the non-progressive hepatic form of type IV glycogen storage disease.

Authors:  A McConkie-Rosell; C Wilson; D A Piccoli; J Boyle; T DeClue; P Kishnani; J J Shen; A Boney; B Brown; Y T Chen
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

8.  Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosis.

Authors:  T T Tang; A D Segura; Y T Chen; L M Ricci; R A Franciosi; M L Splaingard; M S Lubinsky
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

9.  Liver transplantation for type I and type IV glycogen storage disease.

Authors:  R Selby; T E Starzl; E Yunis; S Todo; A G Tzakis; B I Brown; R S Kendall
Journal:  Eur J Pediatr       Date:  1993       Impact factor: 3.183

10.  Neuromuscular forms of glycogen branching enzyme deficiency.

Authors:  C Bruno; D Cassandrini; S Assereto; H Orhan Akman; C Minetti; S Di Mauro
Journal:  Acta Myol       Date:  2007-07
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