[CASE CONTRIBUTIONS TO CHROMOSOMICALLY ACERTAINED KLINEFELTER'S SYNDROME].
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Child↗
Biomedical subjects
G SEGNI
Publications and source records attributed to G SEGNI.
[CONGENITAL ADRENAL HYPERPLASIA. CLINICAL, DIAGNOSTIC AND THERAPEUTIC CONSIDERATIONS APROPOS OF 5 CASES].
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Adrenal Hyperplasia, Congenital↗
[RELATIONSHIP BETWEEN METABOLISM OF TRYPTOPHAN AND PYRIDOXIN IN PHENYLKETONURIA].
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Humans↗
[HEMATOLOGIC ALTERATIONS IN GARGOYLISM].
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Bone Marrow Examination↗
[ON A NEW RAPID TEST FOR BIOLOGIC DIAGNOSIS OF GARGOYLISM].
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Adolescent↗
HILL-BURTON INTRODUCTION PLANT RATING TECHNIC.
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Accreditation↗
DIAGNOSTIC TEST FOR GARGOYLISM.
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Azoles↗
[CURRENT PROBLEMS IN ERYTHROCYTE DEFICIENCY OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE].
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Erythrocytes↗
[FURTHER CONTRIBUTIONS TO THE ENZYMOPATHY OF FAVISM].
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Aldehyde-Lyases↗
[STUDIES ON NEONATAL HYPOGLYCEMIA. 1. ACTIVITY OF GLUCOSE-6-P PHOSPHATASE IN LIVER OF THE NEWBORN].
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Glucose↗
[The tryptophan tolerance test in early infancy].
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Anemia↗
[A new syndrome: congenital hypopotassemic alkalosis].
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Alkalosis↗
Glucose metabolism in human erythrocytes from normal and fava bean-sensitive subjects.
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Anemia↗
[Unusual diseases which are susceptible to treatment with pyridoxine].
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Hematologic Diseases↗
[Oxidation of triose phosphates in hemolysates of erythrocytes of normal human subjects and those with histories of favism].
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Erythrocytes↗
[The consumption of glucose in normal human subjects and those with a history of favism].
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Biological Phenomena↗
[The fundamental biochemical lesion in cystic fibrosis of the pancreas].
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Cystic Fibrosis↗
["Pyridoxine-dependent convulsions". Ist report in Italian literature].
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Child↗