Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage disease von BROWN, B. I, BROWN, D. H

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Liver Transplantation for Type IV Glycogen Storage Disease von Selby, Rick, Starzl, Thomas E, Yunis, Eduardo, Brown, Barbara I, Kendall, Ross S, Tzakis, Andreas

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Liver transplantation for type I and type IV glycogen storage disease von Selby, R, Starzl, T E, Yunis, E, Todo, S, Tzakis, A G, Brown, B I, Kendall, R S

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A new variant of type IV glycogenosis: Deficiency of branching enzyme activity without apparent progressive liver disease von Greene, Harry L., Brown, Barbara I., McClenathan, Daniel T., Agostini, Rocco M., Taylor, Suzanne R.

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Definitive prenatal diagnosis for type III glycogen storage disease von BING-ZHI YANG, JIA-HUAN DING, BROWN, B. I, YUAN-TSONG CHEN

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Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease von YUAN-TSONG CHEN, JUN-KUN HE, JIA-HUAN DING, BROWN, B. I

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Lack of an α -1,4-Glucan: α -1,4-Glucan 6-glycosyl Transferase in a Case of Type IV Glycogenosis von Brown, Barbara Illingworth, Brown, David H.

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A261 DIRECT ACTING ANTIVIRAL THERAPY IS EFFECTIVE IN RECURRENT HEPATITIS C IN BOTH TREATMENT NAIVE AND EXPERIENCED LIVER TRANSPLANT RECIPIENTS: CLINICAL AUDIT OF THE ATLANTIC MULTI... von Hirsch, G, Miles, M, Peltekian, S E, Kiberd, J, Brown, B I, O’Brien, M, Leonard, J, McKnight, L C, McLeod, M, Laryea, M, Peltekian, K M

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Peripheral nerve in type III glycogenosis: Selective involvement of unmyelinated fiber schwann cells von Powell, Henry C., Haas, Richard, Hall, Christopher L., Wolff, Jon A., Nyhan, William, Brown, Barbara I.

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Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency von Tuchman, Mendel, Brown, Barbara I., Burke, Barbara A., Ulstrom, Robert A.

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D98. Access to Certified Burn Centers in The United States: The Geospatial and Transport Cost of Transfer von Edwards, Shelley R., Brown, Madyson I., Hoppe, Ian C., Humphries, Laura S.

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Oncoplastic Breast Reduction: A Systematic Review of Postoperative Complications von Benedict, Katherine C., Brown, Madyson I., Berry, Hunter A., Berry, Scott M., O’Brien, Robert C., Davis, Jared M.

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Branchiobdellid Annelids and Their Crayfish Hosts: Are They Engaged in a Cleaning Symbiosis? von Brown, Bryan L., Robert P. Creed Jr, Dobson, William E.

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Hepatic fructose-1,6-diphosphatase deficiency. A cause of lactic acidosis and hypoglycemia in infancy von Pagliara, A S, Karl, I E, Keating, J P, Brown, B I, Kipnis, D M

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Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III von Ding, Jia-Huan, de Barsy, T., Brown, Barbara I., Coleman, Rosalind A., Chen, Yuan-Tsong

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Portal diversion for the treatment of glycogen storage disease in humans von Starzl, T E, Putnam, C W, Porter, K A, Halgrimson, C G, Corman, J, Brown, B I, Gotlin, R W, Rodgerson, D O, Greene, H L

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The Canadian Dental Association Dental Health Plan for Children von BROWN, B. ISABEL

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The Routledge Companion to Health Humanities von Crawford, Paul, Brown, Brian, Charise, Andrea

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A comparison of applicants and applications to Canadian medical and dental schools, 1965-66 von Fish, D G, Brown, B I

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The apparent activity in vivo of the lysosomal pathway of glycogen catabolism in cultured human skin fibroblasts from patients with type III glycogen storage disease von Brown, D H, Waindle, L M, Brown, B I

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