Hepatomegaly in utero in type III glycogenosisREIFEN, R. M; NADJARI, M; HURVITZ, H et al.Acta paediatrica scandinavica. 1989, Vol 78, Num 6, pp 954-955, issn 0001-656XArticle

Forbes's Branching Conception of Possible WorldsMILLS, E.Analysis (Oxford). 1991, Vol 51, Num 1, pp 48-50, issn 0003-2638Article

DEBRANCHER DEFICIENCY: NEUROMUSCULAR DISORDER IN 5 ADULTSDIMAURO S; HARTWIG GB; HAYS A et al.1979; ANN. NEUROL.; USA; DA. 1979; VOL. 5; NO 5; PP. 422-436; BIBL. 62 REF.Article

Cornstarch therapy in a patient with type III glycogen storage diseaseBOROWITZ, S. M; GREENE, H. L.Journal of pediatric gastroenterology and nutrition. 1987, Vol 6, Num 4, pp 631-634, issn 0277-2116Article

Pregnancy associated with amylo-1,6-glucosidase deficiency (Forbés disease): case reportCONFINO, E; PAUZNER, D; LIDOR, A et al.British journal of obstetrics and gynaecology (Print). 1984, Vol 91, Num 5, pp 494-497, issn 0306-5456Article

A PROPOS D'UN CAS DE GLYCOGENOSE DE TYPE III. DISCUSSION ET COMPARAISON A LA LITTERATUREONESIPPE JEAN.1979; ; FRA; MONTPELLIER: QUICK PRINT; DA. 1979; 316; 59 P.: ILL.-PL.; 30 CM; BIBL. 60 REF.; TH.: MED/MONTPELLIER/1979Thesis

TYPE III GLYCOGENOSIS PRESENTING AS LIVER DISEASE IN ADULTS WITH ATYPICAL HISTOLOGICAL FEATURESFELLOWS IW; LOWE JS; OGILIVE AL et al.1983; JOURNAL OF CLINICAL PATHOLOGY; ISSN 0021-9746; GBR; DA. 1983; VOL. 36; NO 4; PP. 431-434; BIBL. 9 REF.Article

Glycogen storage disease (type-III)SARKAR, A. K; GHOSH, T; CHOUDHURY, T et al.Indian pediatrics. 1991, Vol 28, Num 9, pp 1058-1061, issn 0019-6061Article

Neuromuscular involvement in glycogen storage disease type IIIMOSES, S. W; GADOTH, N; BASHAN, N et al.Acta paediatrica scandinavica. 1986, Vol 75, Num 2, pp 289-296, issn 0001-656XArticle

LA GLICOGENOSI TIPO III. DESCRIZIONE DI UN CASO. = LA GLYCOGENOSE DE TYPE III. DESCRIPTION D'UN CASTURCHI S; CASTRO F; BECCARI A et al.1977; CLIN. PEDIATR.; ITAL.; DA. 1977; VOL. 59; NO 7; PP. 280-288; ABS. FR. ANGL. ALLEM.; BIBL. 14 REF.Article

GLUCOSE-CONTAINING OLIGOSACCHARIDES IN THE URINE OF PATIENTS WITH GLYCOGEN STORAGE DISEASE TYPE II AND TYPE III.LENNARTSON G; LUNDBLAD A; LUNDSTEN J et al.1978; EUROP. J. BIOCHEM.; GERM.; DA. 1978; VOL. 83; NO 2; PP. 325-334; BIBL. 18 REF.Article

Novel exon 11 skipping mutation in a patient with glycogen storage disease type IIIdSUGIE, H; FUKUDA, T; ITO, M et al.Journal of inherited metabolic disease. 2001, Vol 24, Num 5, pp 535-545, issn 0141-8955Article

Glycogen storage disease type IIISANDEEP KAPOOR; KUMAR, P. S; MATHUR, N. B et al.Indian pediatrics. 1994, Vol 31, Num 10, pp 1288-1291, issn 0019-6061Article

Glycogen storage disease type III with muscle involvement : reappraisal of phenotypic variability and prognosisMOMOI, T; SANO, H; YAMANAKA, C et al.American journal of medical genetics. 1992, Vol 42, Num 5, pp 696-699, issn 0148-7299Article

Debrancher deficiency neuromuscular disorder with pseudohypertrophy in two brothersMARBINI, A; GEMIGNANI, F; SACCARDI, F et al.Journal of neurology. 1989, Vol 236, Num 7, pp 418-420, issn 0340-5354Article

RENAL TUBULAR ACIDOSIS ASSOCIATED WITH THE TYPE III GLYCOGENOSISCOHEN J; FRIEDMAN M.1979; ACTA PAEDIATR. SCAND.; SWE; DA. 1979; VOL. 68; NO 5; PP. 779-782; BIBL. 10 REF.Article

Semantics for Propositional Attitude AscriptionsOPPY, G.Philosophical studies. 1992, Vol 67, Num 1, pp 1-18, issn 0031-8116Article

BROKEN PROMISE GOLD MINE = LA MINE D'OR BROKEN PROMISEBULLOCK DAPHNE.1981; AUST. GEM TREASURE HUNTER; ISSN 0159-6322; AUS; DA. 1981-07; NO 59; PP. 38-40; ILL.Article

Using Precision Prairie Reconstruction to Drive the Native Seeded Species Colonization ProcessGRYGIEL, Carolyn E; NORLAND, Jack E; BIONDINI, Mario E et al.Restoration ecology. 2014, Vol 22, Num 4, pp 465-471, issn 1061-2971, 7 p.Article

Two new mutations in the 3' coding region of the glycogen debranching enzyme in a glycogen storage disease type IIIa Ashkenazi Jewish patientPARVARI, R; SHEN, J; HERSHKOVITZ, E et al.Journal of inherited metabolic disease. 1998, Vol 21, Num 2, pp 141-148, issn 0141-8955Article

RFLPs for linkage analysis in families with glycogen storage disease type IIIMISHORI-DERY, A; BASHAN, N; MOSES, S et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 2, pp 207-210, issn 0141-8955Article

Possible prenatal diagnosis of type III glycogenosisMAIRE, I; MATHIEU, M.Journal of inherited metabolic disease. 1986, Vol 9, Num 1, pp 89-91, issn 0141-8955Article

LES GLYCOGENOSES PRIMITIVES PAR DEFICIT D'UN ENZYME DU METABOLISME DU GLYCOGENE1973; MED. INFANT.; FR.; DA. 1973; VOL. 80; NO 2; PP. 193-206Serial Issue

Glycogen storage disease type IIIALPA, Amin S; KASTURI, L; KULKARNI, A. V et al.Indian pediatrics. 2000, Vol 37, Num 6, pp 670-673, issn 0019-6061Article

A novel point mutation in an acceptor splice site of intron 32 (IVS32 A^-12→G) but no exon 3 mutations in the glycogen debranching enzyme gene in a homozygous patient with glycogen storage disease type IIIbOKUBO, M; HORINISHI, A; NAKAMURA, N et al.Human genetics. 1998, Vol 102, Num 1, pp 1-5, issn 0340-6717Article