[ULCERO-HEMORRHAGIC RECTOCOLITIS IN CHILDREN].
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Child↗
Biomedical subjects
J FREZAL
Publications and source records attributed to J FREZAL.
INTESTINAL GLYCOSIDASE ACTIVITIES IN CONGENITAL MALABSORPTION OF DISACCHARIDES.
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Alcohol Oxidoreductases↗
TRUE HERMAPHRODITISM WITH XX-XY MOSAICISM, PROBABLY DUE TO DOUBLE FERTILIZATION OF THE OVUM.
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17-Hydroxycorticosteroids↗
INTESTINAL DISACCHARIDASE ACTIVITY IN CONGENITAL MALABSORPTION OF SUCROSE AND ISOMALTOSE.
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Biopsy↗
[HOW TO RECOGNIZE AND TREAT HEPATIC GLYCOGENOSIS].
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Child↗
[HOW TO TREAT GROWTH RETARDATION].
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Anabolic Agents↗
[THE DETECTION OF HETEROZYGOTES].
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Blood Group Antigens↗
[THE EXCRETION OF FORMIMINOGLUTAMIC ACID (FIGLU) IN THE "NORMAL" INFANT AND IN STEATORRHEA CAUSED BY DISORDER OF INTESTINAL ABSORPTION].
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Avitaminosis↗
[CLINICAL AND BIOLOGICAL STUDY OF A CASE OF PHEOCHROMOCYTOMA].
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Blood Pressure↗
[RADIOLOGICAL CHANGES OF THE SMALL INTESTINE DURING CELIAC DISEASE IN CHILDREN].
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Celiac Disease↗
ANENECEPHALY IN FRANCE.
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Abnormalities, Severe Teratoid↗
[HERMAPHRODITISM WITH XX-XY KARYOTYPE; GENETIC STUDY OF A CASE].
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Blood Protein Electrophoresis↗
[CONGENITAL ERRORS OF METABOLISM].
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Agammaglobulinemia↗
[FACTOR MAP OUTLINE OF THE X CHROMOSOME].
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Angiomatosis↗
[FOLIC ACID DEFICIENCY IN DISORDERS OF INTESTINAL ABSORPTION IN CHILDREN].
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Avitaminosis↗
[A HEREDITARY ACROPATHIC SYNDROME].
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Foot Diseases↗
[Biopsy of the intestinal mucosa in children. Initial results of a study of the malabsorption syndromes].
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Biopsy↗
[MOSAICS INVOLVING THE X CHROMOSOME IN TURNER'S SYNDROME].
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Chromosomes↗