|
1. |
Syndrome De Marfan Avec Lesions Cardiovasculares |
|
Acta Clinica Belgica,
Volume 23,
Issue 5,
1968,
Page 279-290
LornoyW.,
VinckeJ.,
PannierR.,
VerstraetenJ.,
KunnenM.,
Preview
|
PDF (7438KB)
|
|
摘要:
SummaryThe authors report 4 cases of Marfan’s syndrome with cardiovascular lesions : aortic insufficiency and aneurysm of the ascending aorta (1 case), mitral insufficiency and dilatation of the sinus of Valsalva (1 case), aortic insufficiency (2 cases). The patient presenting aortic insufficiency and aneurysm of the ascending aorta was successfully operated upon. The pathogenesis of the aortic and mitral lesions is discussed. In one patient association with cystinuria and in another with polycystic kidneys was found.
ISSN:1784-3286
DOI:10.1080/17843286.1968.11716687
出版商:Taylor&Francis
年代:1968
数据来源: Taylor
|
2. |
Le Traitement Des Hemophiles Par Le Cryoprecipite* |
|
Acta Clinica Belgica,
Volume 23,
Issue 5,
1968,
Page 291-303
PeetermansM.,
CasmanJ.,
Preview
|
PDF (7071KB)
|
|
摘要:
SummaryThe authors have prepared cryoprecipitate (Red Cross, Antwerp) as indicated by Pool. They have administered this product to 6 hemophiliacs (Stuivenberggasthuis, Antwerp) who totalised 20 hemorrhagic episodes. The assay of factor VIII has been performed according to the method described by Bounameaux. The clinical and laboratory outcome was very satisfactory.
ISSN:1784-3286
DOI:10.1080/17843286.1968.11716688
出版商:Taylor&Francis
年代:1968
数据来源: Taylor
|
3. |
Sensibilite Des Staphylocoques Aux Macrolides Et A La Lincomycine |
|
Acta Clinica Belgica,
Volume 23,
Issue 5,
1968,
Page 304-309
YourassowskyE.,
PrudhommeM.R.,
HawotteM.,
Preview
|
PDF (3492KB)
|
|
摘要:
SummaryCross resistance between erythromycin, oleandomycin and lincomycin ofter occurs with staphylococcus aureus (91 %). Certain strains have a«dissociated resistance». Erythromycin resistant strains are sensitive to oleandomycin and to lincomycin and to lincomycin. The number of sensitive strains may be schematized in the following way : erythromycin
ISSN:1784-3286
DOI:10.1080/17843286.1968.11716689
出版商:Taylor&Francis
年代:1968
数据来源: Taylor
|
4. |
Etude Clinique Et Ferrccinetique D’Un Cas De Thrombccythemie Hemorragique Essentielle |
|
Acta Clinica Belgica,
Volume 23,
Issue 5,
1968,
Page 310-324
FrühlingJ.,
WettendorffP.,
KraytmanM.,
HenryJ.,
Preview
|
PDF (9046KB)
|
|
摘要:
SummaryA new case of primary hemorrhagic thrombocythemia is presented, in which ferrokinetic studies were performed 3 times in different phases of the illness.The 84 years old patient fitted all the clinical and hematological criteria of these disease : repeated spontaneous hemorrhages, splenomegaly, persistent thrombocythemia, severe and prolonged anemia, leukocytes not in excess of 50.000 and a rich bone marrow with pronounced megakaryocytic preponderance.Radioactive phosporous treatment produced several remissions, but the patient died 2 years after the diagnosis was established, showing a transformation to acute monocytic leukemia.The quantitative determinations of iron kinetics in the hemorrhagic phase, in remission and in hematologic relapse showed an highly increased erythropoiesis despite of the existent anemia and an important ineffective erythropoiesis.Therefore, the authors feel that primary hemorrhagic thrombocythemia is a myeloproliferative disorder with a predominant platelet elevation.
ISSN:1784-3286
DOI:10.1080/17843286.1968.11716690
出版商:Taylor&Francis
年代:1968
数据来源: Taylor
|
5. |
Bijnierschorshyperfunctie Bij Een Bronchuscarcinoom Met Een Hoog A.C.T.H.-Gehalte Regressie Na Antimitotische Kombinatietherapie |
|
Acta Clinica Belgica,
Volume 23,
Issue 5,
1968,
Page 325-336
Van HoveW.,
Van Der StraetenM.,
VermeulenA.,
BeelaertsW.,
RoelsH.,
Preview
|
PDF (8239KB)
|
|
摘要:
SummaryA report is presented of a patient with a carcinoma of the lung«oat-cell tumor»with secondary Cushing’s syndrome. An unusual biological finding was the absence of hypokaliemia. After a combined antimitotic treatment, regression was obtained both of tumoral signs and Cushing’s syndrome. Finally, as an evidence for its endocrine activity, a high ACTH content could be demonstrated in the tumor tissue.
ISSN:1784-3286
DOI:10.1080/17843286.1968.11716691
出版商:Taylor&Francis
年代:1968
数据来源: Taylor
|
6. |
L’aldosteronisme Primaire Etude D’Un Cas Et Conceptions Actuelles |
|
Acta Clinica Belgica,
Volume 23,
Issue 5,
1968,
Page 337-347
DemanetJ.C.,
PaduartP.,
DelmezJ.P.,
StaquetM.,
GoldsteinM.,
Preview
|
PDF (6668KB)
|
|
摘要:
SummaryA typical case of primary aldosteronism is presented. It comprises however some particular features : exchangeable potassium was not very low and remained unaltered after the removal of a large adenoma of the left adrenal. Clinical signs of diabetes became paradoxically worse after surgery.Recent methods of diagnosis of primary aldosteronism are discussed. The question of its frequency is considered : recent literature seems to indicate that this condition, despite of Conn’s hypothesis, remains an unfrequent cause of hypertension.
ISSN:1784-3286
DOI:10.1080/17843286.1968.11716692
出版商:Taylor&Francis
年代:1968
数据来源: Taylor
|
|