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Your search keyword '"H. Maechel"' showing total 9 results
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9 results on '"H. Maechel"'

1. [Cirkan-induced chronic diarrhea]

Author

H, Maechel

Subjects
Diarrhea, Flavonoids, Male, Hesperidin, Phytosterols, Ascorbic Acid, Thrombophlebitis, Drug Combinations, Chronic Disease, Chymotrypsin, Humans, Female, Trypsin, Aged, Peptide Hydrolases
Published
1992

4. [Cirkan-induced chronic diarrhea].

Author

Maechel H

Subjects
Aged, Ascorbic Acid therapeutic use, Chronic Disease, Drug Combinations, Female, Flavonoids therapeutic use, Humans, Male, Peptide Hydrolases therapeutic use, Phytosterols therapeutic use, Ascorbic Acid adverse effects, Chymotrypsin, Diarrhea chemically induced, Flavonoids adverse effects, Hesperidin, Peptide Hydrolases adverse effects, Phytosterols adverse effects, Thrombophlebitis drug therapy, Trypsin
Published
1992

5. [Atypical diffuse interstitial calcinosis].

Author

Cremer G, Fardeau M, D'Izarn JJ, Maechel H, Marinier F, and Péquignot H

Subjects
Ankle, Calcinosis pathology, Connective Tissue pathology, Diagnosis, Differential, Hand, Humans, Knee, Leg, Male, Middle Aged, Muscular Diseases diagnosis, Myositis Ossificans diagnosis, Calcinosis diagnosis
Published
1978

6. [Hemoglobinopathies in West-African immigrant workers in France (author's transl)].

Author

Labie D, Amegnizin KP, Wajcman H, Pequignot H, Maechel H, Piéron R, Lesobre B, and Coulaud JM

Subjects
Adult, Africa, Western ethnology, Anemia, Sickle Cell epidemiology, Electrophoresis methods, Erythrocytes cytology, Fetal Hemoglobin analysis, France, Hemoglobin A2 analysis, Hemoglobin C analysis, Hemoglobin, Sickle analysis, Humans, Iron blood, Male, Thalassemia diagnosis, Hemoglobinopathies epidemiology
Abstract

In this paper are brought the results obtained in two Parisian hospitals during a survey of abnormal hemoglobins in 540 immigrant workers coming from Africa, mostly from Mali, Mauritania and Senegal. All the subjects investigated were male and between 20 and 40 years old. The studies were performed following internationally standardized technics. The most frequent abnormalities were: Hb S found in 16.3%, Hb C (6.6%), alpha-thalassemia trait (3.1%) and beta-thalassemia trait (3.1%). Some rare abnormalities were also found: delta-chain variants, hereditary persistance of foetal hemoglobin, Hb Hope and Hb Grady. This work emphasizes the high frequency of the different hemoglobin disorders in this population. The easy diagnostic of electrophoretically detectable variants is compared to the more complex situation of thalassemia leading probably to an under estimation of the percentage.

Published
1978

8. [Arteriovenous fistula of the large abdomino-pelvic vessels].

Author

Péquignot H, Chapuis Y, Maechel H, Bonnin A, Bleichner G, and Travagli JP

Subjects
Adult, Female, Heart Diseases etiology, Humans, Iliac Artery surgery, Iliac Vein surgery, Arteriovenous Malformations complications, Arteriovenous Malformations surgery, Iliac Artery abnormalities, Iliac Vein abnormalities
Published
1978

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