The 27-day recurrence tendency in the muon intensity of cosmic radiation measured at 40 m w.e. underground

1962 ◽  
Vol 24 (2) ◽  
pp. 316-323 ◽  
Author(s):  
T. Sándor ◽  
A. Somogyi ◽  
P. Telbisz
Keyword(s):  
Cosmic Radiation ◽  
Muon Intensity ◽  
Recurrence Tendency

Anisotropies in Cosmic Radiation

Tellus ◽  
1959 ◽  
Vol 11 (2) ◽  
pp. 239-248 ◽  
Author(s):  
A. Dattner ◽  
D. Venkatesan
Keyword(s):  
Cosmic Radiation

The cosmic radiation effects and activation monitor

1989 ◽  
Author(s):  
C. S. Dyer ◽  
A. J. Sims ◽  
R. J. Hutchings ◽  
D. Mapper ◽  
J. H. Stephen ◽  
...  
Keyword(s):  
Cosmic Radiation ◽  
Radiation Effects

A model method for testing cosmic radiation

1973 ◽  
Vol 15 (6) ◽  
pp. 430-432
Author(s):  
M. Sosna
Keyword(s):  
Cosmic Radiation ◽  
Model Method

scholarly journals Cosmic radiation does not prevent collisional charging in (pre)-planetary atmospheres

Icarus ◽  
2021 ◽  
Vol 355 ◽  
pp. 114127
Author(s):  
Felix Jungmann ◽  
Tetyana Bila ◽  
Laura Kleinert ◽  
Andre Mölleken ◽  
Rolf Möller ◽  
...  
Keyword(s):  
Cosmic Radiation ◽  
Planetary Atmospheres

scholarly journals A solitary giant neurofibroma of inguinal region: A case report

2021 ◽  
Vol 104 (1) ◽  
pp. 003685042110042
Author(s):  
Haiying Zhou ◽  
Hui Lu
Keyword(s):  
Tumor Resection ◽  
Clinical Manifestations ◽  
Inguinal Region ◽  
Nerve Sheath Tumor ◽  
Neurogenic Tumors ◽  
Long Time ◽  
Giant Neurofibroma ◽  
History Of ◽  
Neuroectodermal Origin ◽  
Recurrence Tendency

Neurofibroma is a rare nerve sheath tumor of neuroectodermal origin, especially the huge and isolated neurofibroma located in the inguinal region. To our knowledge, no such case has previously been reported. We report a case of 34-year-old male patient with a 4-year history of progressive enlargement of the medial root mass in his left thigh with sitting and standing disorders along with pain. The tumor was completely removed by operation, and pathological diagnosis showed neurofibroma. There was no obvious neurologic defect after surgery, and no recurrence tendency was found in the follow-up of 2 years. For a large solitary mass with slow growth and no malignant clinical manifestations for a long time, clinicians cannot rule out the hypothetical diagnosis of neurofibroma, even though its growth site is very rare, such as this case of a huge tumor located in the groin. For neurogenic tumors, early operation should be performed, and the prognosis of patients after tumor resection is excellent.

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