A biochemical abnormality found in muscle from unstressed malignant-hyperpyrexia-susceptible humans

1984 ◽  
Vol 12 (3) ◽  
pp. 357-358 ◽  
Author(s):  
F. R. ELLIS ◽  
P. J. HALSALL ◽  
P. ALLAM ◽  
E. HAY
1977 ◽  
Vol 2 (23) ◽  
pp. 757-758 ◽  
Author(s):  
M. A. Denborough

1973 ◽  
Vol 1 (11) ◽  
pp. 525-528 ◽  
Author(s):  
J. O. KING ◽  
M. A. DENBOROUGH

1972 ◽  
Vol 16 (5) ◽  
pp. 433
Author(s):  
K. KYEI-MENSAH ◽  
R. LOCKWOOD ◽  
J. H. TYRELL ◽  
I. H. WILLETT

1972 ◽  
Vol 16 (1) ◽  
pp. 33
Author(s):  
P. M. E. DRURY ◽  
A. A. GILBERTSON

BMJ ◽  
1969 ◽  
Vol 1 (5642) ◽  
pp. 488-488 ◽  
Author(s):  
B. R. Murray ◽  
P. A. Williams

2009 ◽  
Vol 15 (3) ◽  
pp. 181-191 ◽  
Author(s):  
Niraj Ahuja ◽  
Andrew J. Cole

SummaryPresence of fever in psychiatric patients may signify a number of potentially fatal conditions. Several of these are related to treatments (e.g. neuroleptic malignant syndrome with antipsychotics, serotonin syndrome with serotonergic antidepressants, and malignant hyperpyrexia with anaesthesia used for administration of electroconvulsive therapy) or exacerbated by them (e.g. malignant catatonia with antipsychotics). New classes of drug treatment may be changing the epidemiology of these disorders. We suggest that an initial diagnosis of hyperthermia syndrome is clinically useful as there are some important commonalities in treatment. We outline a systematic approach to identify a particular subtype of hyperthermia syndrome and the indications for more specific treatments where available.


PEDIATRICS ◽  
1969 ◽  
Vol 44 (5) ◽  
pp. 655-660
Author(s):  
Bernard E. Cohen ◽  
Arieh Szeinberg ◽  
Wifred Berman ◽  
Yermiahu Aviad ◽  
Moshe Crispin ◽  
...  

A highly inbred family with five mentally retarded persons is described. Two sibs presented typical characteristics of phenylketonuria, while one mentally retarded sib did not show any biochemical abnormality. The mother and maternal uncle had mild hyperphenylalaninemia. It is pointed out in the discussion that, while the mental retardation (at least in some of these subjects) may be independent of disturbances of phenylalanine metabolism, it is possible also to explain all the findings in the family on a unified basis, involving a variant hyperphenylalaninemia with tolerance increasing with age and "maternal phenylketonuia."


PEDIATRICS ◽  
1976 ◽  
Vol 57 (4) ◽  
pp. 474-479
Author(s):  
Robert B. Elliott

Seven children with cystic fibrosis (CF) have been treated for at least one year with intravenously administered soya oil emulsion. In all, an improvement of at least one biochemical abnormality in character with the disease appeared. The children's clinical course remains benign. This course is remarkably better than that of other children with CF treated without Intralipid in Auckland in the same period, though a placebo effect cannot be discounted. It is postulated that intravenous supplementation with essential fatty acid in CF may in turn partially correct an error of metabolism of prostaglandins present in the disease.


1976 ◽  
Vol 20 (3) ◽  
pp. 246???247
Author(s):  
B. Peltz ◽  
J. Carstens

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