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British Journal of Pharmacology, EarlyView.Abstract Background and Purpose Immune checkpoint inhibitors (ICI) have revolutionized cancer therapy, offering improvements in survival across various malignancies. However, their toxicities pose a major challenge for cardio‐oncology units. Despite their growing importance, data on effectiveness of such specialized units in mitigating ICI‐associated ...
Elias Haj‐Yehia +6 more
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Lille medical : journal de la Faculte de medecine et de pharmacie de l'Universite de Lille, 1996
The exact incidence of West’s syndrome is difficult to determine, as it merges with other types of epilepsy, of which there are many. It is only when specific tests are carried out, and the results added to the typical clinical signs, that this syndrome can be distinguished.
J P, FARRIAUX, P, DELMAS
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The exact incidence of West’s syndrome is difficult to determine, as it merges with other types of epilepsy, of which there are many. It is only when specific tests are carried out, and the results added to the typical clinical signs, that this syndrome can be distinguished.
J P, FARRIAUX, P, DELMAS
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Journal of Child Neurology, 2002
West's syndrome (infantile spasms) can be considered the classic disorder of the catastrophic childhood epilepsies. Although West's syndrome was identified 160 years ago, it is still not fully understood today. Because of the multiple etiologies associated with West's syndrome, the evaluation and treatment of the disease are complex, and, to date ...
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West's syndrome (infantile spasms) can be considered the classic disorder of the catastrophic childhood epilepsies. Although West's syndrome was identified 160 years ago, it is still not fully understood today. Because of the multiple etiologies associated with West's syndrome, the evaluation and treatment of the disease are complex, and, to date ...
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Leigh syndrome associated with West syndrome
Brain and Development, 2003Leigh syndrome (LS) (sub-acute necrotizing encephalomyelopathy) is characterized by symmetric brain lesions occurring mainly in the basal ganglia and associated with variable clinical manifestations such as hypotonia, psychomotor retardation, and feeding difficulties. Patients with LS may develop seizures.
Masahiro, Tsuji +6 more
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Familial Idiopathic West Syndrome
Journal of Child Neurology, 2000Two families, each with occurrence of West syndrome in two siblings, are presented. Monozygotic twins in family 1 developed infantile spasms at the age of 4 months. Two female siblings in family 2 started to have seizures at the age of 6 months, but 2 years apart.
E, Reiter +5 more
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West syndrome associated with mosaic Down syndrome
Brain and Development, 2007We report a girl with West syndrome associated with mosaic Down syndrome. She had repetitive tonic spasms at 6 months and an electroencephalography (EEG) showed hypsarrhythmia. Her facial appearance was normal and she had no minor anomalies. Her karyotype was mosaic(46,XX/47,XX,+21).
Madoka, Kajimoto +5 more
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Brain and Development, 2011
West syndrome is one of the most refractory epileptic syndromes in infancy, and many researchers have made great effort to find optimal treatment modalities for this syndrome. In this review, previous literature on optimal treatments of West syndrome and its refractory nature were briefly presented, followed by an introduction of recent publication of ...
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West syndrome is one of the most refractory epileptic syndromes in infancy, and many researchers have made great effort to find optimal treatment modalities for this syndrome. In this review, previous literature on optimal treatments of West syndrome and its refractory nature were briefly presented, followed by an introduction of recent publication of ...
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Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1992
West-Syndrome is an age-dependent early epileptic encephalopathy manifesting during the first year of life. It carries a high risk for an unfavourable longterm prognosis, especially for the prevailing group of patients with the symptomatic form. Etiologically associated factors are heterogeneous.
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West-Syndrome is an age-dependent early epileptic encephalopathy manifesting during the first year of life. It carries a high risk for an unfavourable longterm prognosis, especially for the prevailing group of patients with the symptomatic form. Etiologically associated factors are heterogeneous.
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PERIVENTRICULAR LEUKOMALACIA AND WEST SYNDROME
Developmental Medicine & Child Neurology, 1996SUMMARYThe authors studied the clinical course and electroencephalograms (ÉEGs) of 27 patients with periventricular leukomalacia (PVL), to investigate the relation betwéen PVL and West syndrome. Seven of the 27 patients with PVL developed WS; in all seven the PVL was severe. Bilateral parieto‐occipital dominant irregular polyspike‐and‐wave (PO‐polySpW)
A, Okumura +3 more
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