Inborn Disorders of Sphingolipid Metabolism. Proceedings of the Third International Symposium on the Cerebral Sphingolipidoses

Content: 
Front Matter, Page iii
Copyright, Page iv
PREFACE, Page v, S.M.A., B.W.V.
ACKNOWLEDGMENTS, Page vii, Abner Wolf, Warren M. Sperry, Bruno W. Volk, Jordi Folch-Pi, Harry M. Zimmerman
CONTRIBUTORS AND PARTICIPANTS, Pages xiii-xvi
ELECTRON MICROSCOPIC OBSERVATIONS IN BATTEN'S DISEASE, Pages 3-22, SHEILA DONAHUE, WOLFGANG ZEMAN, ITARU WATANABE
JUVENILE FORM OF AMAUROTIC FAMILY IDIOCY. A CONTRIBUTION TO THE MORPHOLOGICAL, HISTOCHEMICAL AND ELECTRON-MICROSCOPIC ASPECTS, Pages 23-42, PAUL B. DIEZEL, JOHANNES A. ROSSNER, N. KOPPANG, PETER RITZHAUPT, DIETER BARTLING
THE MYOCLONIC VARIANT OF CEREBRAL LIPIDOSIS, Pages 43-74, FRANZ SEITELBERGER, HANS JACOB, RALF SCHNABEL
ANATOMO-CHEMICAL STUDY OF THE WHITE MATTER IN LATE INFANTILE AMAUROTIC IDIOCY, Pages 75-91, G.W.F. EDGAR, LUDO VAN BOGAERT
THE FINE STRUCTURE OF THE BRAIN AND OTHER ORGANS IN NIEMANN–PICK DISEASE, Pages 93-105, SARAH LUSE
ELECTRON MICROSCOPIC AND HISTOCHEMICAL STUDIES OF VISCERA IN LIPIDOSES, Pages 107-120, BARBARA J. WALLACE, SYDNEY S. LAZARUS, BRUNO W. VOLK
LUXOL-DYE STAINING IN LIPID STORAGE DISEASES, Pages 121-128, BENJAMIN H. LANDING, JOHN S. O'BRIEN, LIANNE G. WILCOX
STUDIES ON SPONGY DEGENERATION OF THE CENTRAL NERVOUS SYSTEM (VAN BOGAERT–BERTRAND TYPE), Pages 129-147, MASAZUMI ADACHI, STANLEY M. ARONSON
THE SYNDROME OF FAMILIAL LEUKODYSTROPHY, ADRENAL INSUFFICIENCY AND CUTANEOUS MELANOSIS, Pages 149-166, MARY JANE AGUILAR, JOHN S. O'BRIEN, PADDY TABER
THE METABOLISM OF GANGLIOSIDES IN CEREBRAL LIPIDOSES, Pages 169-186, LARS SVENNERHOLM
STUDIES ON THE BIOSYNTHESIS OF GANGLIOSIDES, Pages 187-192, JULIAN N. KANFER, ROSCOE O. BRADY
STUDIES ON THE BIOSYNTHESIS OF GANGLIOSIDES, Pages 193-213, BERNARD KAUFMAN, SUBHASH BASU, SAUL ROSEMAN
GANGLIOSIDE PATTERNS OF NORMAL AND PATHOLOGICAL BRAINS, Pages 215-230, KUNIHIKO SUZUKI
STRUCTURAL STUDIES OF THE TAY–SACHS GANGLIOSIDE AND ITS NORMAL BRAIN COUNTERPART, Pages 231-240, ROBERT LEDEEN, KENNETH SALSMAN, MARIA CABRERA
ISOLATION AND STRUCTURAL ANALYSIS OF BRAIN GANGLIOSIDES, Pages 241-250, R.H. MCCLUER, R.J. PENICK
THE METABOLISM OF SIALIC ACIDS, Pages 251-259, LEONARD WARREN
COMPARISON OF FOUR ENZYMES FROM BRAIN WHICH HYDROLYZE SPHINGOLIPIDS, Pages 261-266, SHIMON GATT
THE NATURE OF THE LIPOPHILIC PORTIONS OF THE BRAIN GANGLIOSIDES, Pages 267-272, ABRAHAM ROSENBERG
BRAIN PROTEINS IN THE SPHINGOLIPIDOSES: TAY–SACHS DISEASE PROTEIN, Pages 273-287, SAMUEL BOGOCH, PETER BELVAL
COMPARATIVE STUDIES OF NORMAL HUMAN AND TAY–SACHS GANGLIOSIDES—AN IMMUNOCHEMICAL APPROACH, Pages 289-301, THERESA A. PASCAL, ABRAHAM SAIFER, JOSEPH GITLIN
VARIATIONS IN LIPID COMPOSITION OF HUMAN BRAIN DURING DEVELOPMENT AND IN THE SPHINGOLIPIDOSES: USE OF TWO-DIMENSIONAL THIN-LAYER CHROMATOGRAPHY, Pages 303-316, GEORGE ROUSER, GENE KRITCHEVSKY, CLAUDIO GALLI, AKIRA YAMAMOTO, ALFRED G. KNUDSON JR.
THE FORMATION OF MEMBRANE AGGREGATES, Pages 317-324, S. SAMUELS, F. ALEU
DETERMINATION OF THE LIPID BASES IN THE LIPIDS OF SPINAL CORD, OPTIC NERVE AND SCIATIC NERVE OF SOME SPECIES, Pages 325-337, G. SCHMIDT, E.L. HOGAN, A. KJETA-FYDA, T. TANAKA, J. JOSEPH, N.I. FELDMAN, R.A. COLLINS, R.W. KEENAN
CEREBROSIDE METABOLISM IN EXPERIMENTAL PHENYLKETONURIA AND GALACTOSEMIA, Pages 339-357, TOHRU INOUYE, PARVIN JUSTICE, DAVID YI-YUNG HSIA
SOME RECENT FINDINGS IN LEUKODYSTROPHIES AND IN GARGOYLISM, Pages 359-387, JAMES H. AUSTIN
ISOLATION AND CHARACTERIZATION OF THE PRINCIPAL CEREBRAL GLYCOLIPIDS IN THE INFANTILE AND ADULT FORMS OF GAUCHER'S DISEASE, Pages 389-400, MICHEL PHILIPPART, JOHN H. MENKES
CLINICAL MANIFESTATIONS OF TAY–SACHS DISEASE AND NIEMANN–PICK DISEASE, Pages 403-411, LARRY SCHNECK, BRUNO W. VOLK
THE SLEEP–DREAM PATTERN IN TAY–SACHS DISEASE (PRELIMINARY OBSERVATIONS), Pages 413-421, I. KARACAN, L. SCHNECK, L.P. HINTERBUCHNER, K. GROSS
ON THE CHEMICAL CHANGES IN THE RED CELL STROMA IN TAY–SACHS DISEASE: THEIR VALUE AS GENETIC TRACERS, Pages 423-430, JOHN A. BALINT, EMILIOS C. KYRIAKIDES, HUGH L. SPITZER
REPRODUCTIVE FITNESS AND SELECTION IN TAY–SACHS DISEASE, Pages 431-441, NTINOS C. MYRIANTHOPOULOS, STANLEY M. ARONSON
PERSISTENCE OF A METABOLIC DEFECT IN TISSUE CULTURES DERIVED FROM PATIENTS WITH NIEMANN–PICK DISEASE, Pages 443-453, B. WILLIAM UHLENDORF, ALBERT I. HOLTZ, MICHAEL B. MOCK, DONALD S. FREDRICKSON
STUDIES ON THE GENETICS OF THE HURLER–HUNTER SYNDROME, Pages 455-473, JULES G. LEROY, ALLEN C. CROCKER
LEUKOCYTIC HYPERGRANULATION VERSUS LYMPHOCYTIC VACUOLIZATION AS MARKERS FOR HETEROZYGOTES AND HOMOZYGOTES WITH BATTEN–SPIELMEYER–VOGT DISEASE, Pages 475-484, WOLFGANG ZEMAN, JONAS C. STROUTH
THE “LIPOGRANULOMATOSIS” SYNDROME; REVIEW, WITH REPORT OF PATIENT SHOWING MILDER INVOLVEMENT, Pages 485-503, ALLEN C. CROCKER, JONATHAN COHEN, SIDNEY FARBER
SUMMARY REMARKS, Pages 505-508, GEORGE A. JERVIS
INDEX, Pages 509-513