Results 61 to 70 of about 26,625,900 (87)

Functional outcome after Swenson′s operation for Hirshsprung′s disease

, 2010
Background/Aim: Hirschsprung′s disease (HD) is one of the most common causes resulting in lower intestinal obstruction in children with atypical clinical symptoms and inconspicuous morphological findings by barium enema X-ray.
AbdEl Bary Hala, AbdEl Messeh Magdy, Gad El-Hak Nabil, Negm Emad, El-Hemaly Mohamed, El-Hanafy Ehab   +5 more
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Meniere′s disease: Still a mystery disease with difficult differential diagnosis

, 2011
One hundred and forty-six years after its first description, the differential diagnosis of Meniere′s disease remains very challenging. The aim of the present study is to review the current knowledge on the advantages and disadvantages of the new ...
Vassiliou A, Candiloros D, Maragoudakis P, Nikolopoulos T, Vlastarakos P   +4 more
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Limited wegener′s granulomatosis presenting as multiple retinal vascular occlusions

, 2002
In the early stages of Wegener′s granulomatosis, and in the atypical forms, the classic clinicopathologic features of the disease are often absent, delaying diagnosis.
Siyabi Huda, Amer Ali, Shenoy Radha, Elagib El Nour   +3 more
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Membranoproliferative glomerulonephritis in the setting of multicentric angiofollicular lymph node hyperplasia (Castleman's disease) complicated by Evan's syndrome

, 2010
Systemic Castleman's disease is a lymphoproliferative disorder with various clinical presentations and incompletely understood aetiology. The authors report on a rare case of the plasma cell variant of Castleman's disease associated with ...
Patsouris, E., Lelouda, M., Lazaris, A.C., Stofas, A., Paraskevakou, H., Marinaki, S., Gakiopoulou, H., Voulgarelis, M., Boletis, J., Korkolopoulou, P.   +9 more
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A rare association of Castleman′s disease and nephrotic syndrome

, 2011
Castleman′s Disease (CD) is an uncommon and poorly understood disorder of lymph node hyperplasia of unknown etiology. This entity belongs to the atypical lymphoproliferative disorders, a heterogeneous group of diseases characterized by a hyperplastic ...
M Rachid, A Quessar, S Benchekroun, I Tazi   +3 more
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Hypokalemic paralysis due to primary hyperaldosteronism simulating gitelman′s syndrome

, 2009
Some diseases, such as Gitelman′s syndrome, Bartter′s syndrome, and primary hyperaldosteronism (Conn′s syndrome), may bear some similar clinical and laboratory findings.
Kasifoglu Timucin, Cansu Dondu, Akalin Aysen, Korkmaz Cengiz   +3 more
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Optic Neuritis in Castleman Disease

, 2008
The aim of this manuscript is to report the occurrence of optic neuritis in a patient with Castleman ...
Ungsoo Kim; Jeong-Min Hwang
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Fournier′s gangrene of the penis

, 2005
Fournier′s gangrene is a rare, fulminant, though generally localized disease of the scrotum and penis with occasional extension up the abdominal wall. The usual organism is an anaerobic streptococcus synergistic with some second organism. Our case
Roshan M, Ravikrishnan J, Tauro Leo, Menezes Leo, Satish Rao B   +4 more
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Hirschsprung′s disease: Management problem in a developing country

, 2010
Background: The management of Hirschsprung′s disease remains a problem in developing countries. Our aim is to identify the main epidemiological, clinical, and therapeutic characteristics of Hirschsprung′s disease at the University Child ...
Wandaogo A, Tapsoba T, Kaboré R.A.F, Bambara C, Soré O, Bandré E, Ouedraogo I   +6 more
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Malignant syndrome in Parkinson′s disease without dopaminergic drug withdrawal

, 2008
Malignant syndrome is a rare complication occurring during the course of drug treatment for Parkinson′s disease. It resembles neuroleptic malignant syndrome and is characterized by fever, marked rigidity, altered consciousness, leucocytosis and ...
Suresh Chandran C
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