Inherited Agammaglobulinemia with Malabsorption and Marked Alterations in the Gastrointestinal Mucosa
- 12 January 1963
- journal article
- Published by Wiley in Acta Medica Scandinavica
- Vol. 173 (5), 549-555
- https://doi.org/10.1111/j.0954-6820.1963.tb17439.x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- DIAGNOSIS OF HYPOGAMMAGLOBULINEMIAJAMA, 1962
- Primary Acquired Agammaglobulinemia, with a Family History of Collagen Disease and Hematologic DisordersNew England Journal of Medicine, 1962
- Clinical Investigation of Patients with Agammaglobulinemia and HypogammaglobulinemiaPediatric Clinics of North America, 1960
- Coeliac Disease: Histopathological Findings in the Small Intestinal Mucosa Studied by a Peroral Biopsy TechniqueGut, 1960
- A Multipurpose Instrument for Suction Biopsy of the Esophagus, Stomach, Small Bowel, and ColonGastroenterology, 1959
- Some Observations on the Malabsorption Syndrome, Based on the Use of Absorption Tests and Biopsy of the Small IntestineGastroenterology, 1959
- Primary malabsorption syndrome—past, present and futureDigestive Diseases and Sciences, 1959
- Agammaglobulinemia in the adultAmerican Journal Of Medicine, 1955
- Absence of Serum Gamma Globulins in an AdultNew England Journal of Medicine, 1954
- Dystrophia myotonica with associated sprue-like symptomsAmerican Journal Of Medicine, 1954