Elizabeth F. Neufeld

Elizabeth F. Neufeld's AcademicInfluence.com Rankings

Biology

#3487

World Rank

#5328

Historical Rank

#1407

USA Rank

Genetics

#300

World Rank

#353

Historical Rank

#136

USA Rank

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Biology

Why Is Elizabeth F. Neufeld Influential?

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According to Wikipedia, Elizabeth Fondal Neufeld is a French-American geneticist whose research has focused on the genetic basis of metabolic disease in humans. Life Neufeld and her Russian Jewish family emigrated to the United States from Paris in 1940; they had left Europe as refugees to escape Nazi persecution. The family settled in New York, where she attended Hunter College High School before graduating from Queens College in 1948 with a Bachelor of Science. She went on to work as a research assistant at the Jackson Laboratory in Bar Harbor, Maine, looking at blood disorders in mice. Later on, she attended graduate school at University of California, Berkeley, where she earned a Ph.D. in 1956 for her work on nucleotides and complex carbohydrates.

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Elizabeth F. Neufeld's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

MODERN METHODS OF PLANT ANALYSIS (1955) (2109)
CARBOHYDRATE METABOLISM. (1965) (943)
Enzyme-replacement therapy in mucopolysaccharidosis I. (2001) (636)
Biosynthesis of lysosomal enzymes in fibroblasts. Synthesis as precursors of higher molecular weight. (1980) (582)
Hurler and Hunter Syndromes: Mutual Correction of the Defect in Cultured Fibroblasts (1968) (422)
Activated microglia in cortex of mouse models of mucopolysaccharidoses I and IIIB (2003) (403)
A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomes. (1972) (393)
Lysosomal storage diseases. (1991) (380)
Biosynthesis of lysosomal enzymes in fibroblasts. Phosphorylation of mannose residues. (1980) (335)
Lysosomal storage diseases (2018) (335)
Inherited disorders of lysosomal metabolism. (1975) (283)
Two species of lysosomal organelles in cultured human fibroblasts (1979) (278)
The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide. (1968) (268)
Recognition and receptor-mediated uptake of a lysosomal enzyme, α-l-iduronidase, by cultured human fibroblasts (1977) (265)
THE FEEDBACK CONTROL OF SUGAR NUCLEOTIDE BIOSYNTHESIS IN LIVER. (1964) (264)
A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts. (1974) (242)
The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase. (1972) (217)
Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase. (1999) (209)
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. (1973) (195)
Inborn errors of mucopolysaccharide metabolism. (1970) (195)
Carbohydrate Recognition Systems for Receptor-Mediated Pinocytosis (1980) (190)
The transport of lysosomal enzymes. (1977) (190)
Long-term and high-dose trials of enzyme replacement therapy in the canine model of mucopolysaccharidosis I. (1996) (174)
CORRECTIVE FACTORS FOR INBORN ERRORS OF MUCOPOLYSACCHARIDE METABOLISM (1971) (170)
Enzyme replacement in a canine model of Hurler syndrome. (1994) (162)
The defect in Hurler and Hunter syndromes. II. Deficiency of specific factors involved in mucopolysaccharide degradation. (1969) (155)
Synthesis of a beta-1, 3-linked glucan by extracts of Phaseolus aureus seedlings. (1958) (153)
Pyridine nucleotide transhydrogenase. III. Animal tissue transhydrogenases. (1953) (153)
Is there a mechanism for introducing acid hydrolases into liver lysosomes that is independent of mannose 6-phosphate recognition? Evidence from I-cell disease. (1982) (150)
Aptamer-based endocytosis of a lysosomal enzyme (2008) (146)
Biosynthesis and turnover of the mannose 6-phosphate receptor in cultured Chinese hamster ovary cells. (1983) (137)
Natural history and inherited disorders of a lysosomal enzyme, beta-hexosaminidase. (1989) (134)
Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy (2009) (128)
The molecular basis of Sanfilippo syndrome type B. (1996) (127)
The Sanfilippo A corrective factor. Purification and mode of action. (1972) (124)
A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblasts. (1973) (121)
INHIBITION OF UDP-D-GLUCOSE DEHYDROGENASE BY UDP-D-XYLOSE: A POSSIBLE REGULATORY MECHANISM. (1965) (118)
Association of alpha- and beta-subunits during the biosynthesis of beta-hexosaminidase in cultured human fibroblasts. (1984) (115)
Allelism, non-allelism, and genetic compounds among the mucopolysaccharidoses. (1972) (111)
Intrauterine diagnosis of the hurler and hunter syndromes. (1969) (109)
Morphologic study of the internalization of a lysosomal enzyme by the mannose 6-phosphate receptor in cultured Chinese hamster ovary cells. (1981) (109)
Human beta-hexosaminidase alpha chain: coding sequence and homology with the beta chain. (1985) (109)
The 4-epimerization and decarboxylation of uridine diphosphate D-glucuronic acid by extracts from Phaseolus aureus seedlings. (1960) (107)
METABOLISM OF MYO-INOSITOL IN PLANTS: CONVERSION TO PECTIN, HEMICELLULOSE, D-XYLOSE, AND SUGAR ACIDS. (1962) (106)
Formation and interconversion of sugar nucleotides by plant extracts. (1957) (102)
Pyridine nucleotide transhydrogenase. I. Indirect evidence for the reaction and purification of the enzyme. (1952) (101)
Comparison of Normal Blood Picture of Young Adults from 18 Inbred Strains of Mice (1951) (99)
Lysosomal accumulation of SCMAS (subunit c of mitochondrial ATP synthase) in neurons of the mouse model of mucopolysaccharidosis III B. (2007) (96)
Direct demonstration of binding of a lysosomal enzyme, alpha-L-iduronidase, to receptors on cultured fibroblasts. (1979) (96)
Architecture of the canine IDUA gene and mutation underlying canine mucopolysaccharidosis I. (1992) (94)
Nonsense-Mediated Decay of HumanHEXA mRNA (2001) (92)
Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients in Israel: multiple allelic mutations of the IDUA gene in a small geographic area. (1993) (90)
A frameshift mutation in a patient with Tay-Sachs disease causes premature termination and defective intracellular transport of the alpha-subunit of beta-hexosaminidase. (1989) (88)
Overexpression of the Human Lysosomal Enzyme α-L-Iduronidase in Chinese Hamster Ovary Cells (1994) (86)
Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I. (1982) (86)
Attenuated plasticity in neurons and astrocytes in the mouse model of Sanfilippo syndrome type B (2002) (86)
The Hurler corrective factor. Purification and some properties. (1971) (85)
Treatment of the mouse model of mucopolysaccharidosis I with retrovirally transduced bone marrow. (2003) (85)
Molecular basis of adult-onset and chronic GM2 gangliosidoses in patients of Ashkenazi Jewish origin: substitution of serine for glycine at position 269 of the alpha-subunit of beta-hexosaminidase. (1989) (85)
Delivery of an enzyme-IGFII fusion protein to the mouse brain is therapeutic for mucopolysaccharidosis type IIIB (2014) (82)
Morphologic and biochemical studies of canine mucopolysaccharidosis I. (1984) (82)
α-l-Iduronidase activity in cultured skin fibroblasts and amniotic fluid cells (1973) (81)
Inhibition of receptor-mediated uptake of a lysosomal enzyme into fibroblasts by chloroquine, procaine and ammonia. (1979) (78)
Synthesis of beta-hexosaminidase in cell-free translation and in intact fibroblasts: an insoluble precursor alpha chain in a rare form of Tay-Sachs disease. (1982) (78)
Formation of galactolipids by chloroplasts. (1964) (76)
Complex heterosaccharides of animals. (1969) (76)
A canine model of human alpha-L-iduronidase deficiency. (1983) (74)
Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening program. (1990) (74)
Scheie and Hurler Syndromes: Apparent Identity of the Biochemical Defect (1970) (74)
Pyridine nucleotide transhydrogenase. II. Direct evidence for and mechanism of the transhydrogenase reaction. (1952) (74)
Glycosylation of serine residues by a uridine diphosphate-xylose: protein xylosyltransferase from mouse mastocytoma. (1966) (69)
Biochemical heterogeneity of the Sanfilippo syndrome: preliminary characterization of two deficient factors. (1971) (66)
BIOSYNTHESIS OF SACCHARIDES FROM GLYCOPYRANOSYL ESTERS OF NUCLEOTIDES ("SUGAR NUCLEOTIDES"). (1963) (65)
Molecular order in mucolipidosis II and III nomenclature (2008) (60)
Synthesis of galactosylinositol by extracts from peas. (1963) (60)
Juvenile GM2 gangliosidosis caused by substitution of histidine for arginine at position 499 or 504 of the alpha-subunit of beta-hexosaminidase. (1990) (59)
Purification and Characterization of Recombinant Human α-N-Acetylglucosaminidase Secreted by Chinese Hamster Ovary Cells (2000) (59)
Iduronate Sulfatase Activity in Serum, Lymphocytes, and Fibroblasts—Simplified Diagnosis of the Hunter Syndrome (1976) (57)
NAGLU mutations underlying Sanfilippo syndrome type B. (1998) (56)
Maturation of alpha-L-iduronidase in cultured human fibroblasts. (1981) (56)
SUGAR NUCLEOTIDES IN THE INTERCONVERSION OF CARBOHYDRATES IN HIGHER PLANTS. (1959) (55)
Retrovirally transduced bone marrow has a therapeutic effect on brain in the mouse model of mucopolysaccharidosis IIIB. (2004) (53)
The Hunter corrective factor. Purification and preliminary characterization. (1972) (51)
Phosphorylation of D-galactose and L-arabinose by extracts from Phaseolus aureus seedlings. (1960) (50)
An assay for iduronate sulfatase (Hunter corrective factor). (1974) (48)
Carbohydrate Structures of Recombinant Human α-l-Iduronidase Secreted by Chinese Hamster Ovary Cells* (1997) (48)
Two mutations produce intron insertion in mRNA and elongated beta-subunit of human beta-hexosaminidase. (1990) (48)
Cloning and characterization of cDNA encoding canine alpha-L-iduronidase. mRNA deficiency in mucopolysaccharidosis I dog. (1992) (47)
Enzymic synthesis of uridine diphosphate glucuronic acid and uridine diphosphate galacturonic acid with extracts from Phaseolus aureus seedlings. (1958) (47)
Incorporation of D-xylose-C14 into glycoprotein by particles from hen oviduct. (1966) (47)
Pyridine nucleotide transhydrogenase. IV. Effect of adenylic acid a on the bacterial transhydrogenases. (1953) (46)
Simulation of genetic mucopolysaccharidoses in normal human fibroblasts by alteration of pH of the medium. (1972) (46)
X-linked Hunter syndrome: the heterozygous phenotype in cell culture. (1977) (45)
Faulty association of alpha- and beta-subunits in some forms of beta-hexosaminidase A deficiency. (1984) (45)
Defects in the Medial Entorhinal Cortex and Dentate Gyrus in the Mouse Model of Sanfilippo Syndrome Type B (2011) (44)
The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency? (1977) (44)
A rapid and sensitive assay for neuraminidase: Application to cultured flbroblasts (1979) (44)
The uptake of enzymes into lysosomes: an overview. (1980) (44)
ENZYMATIC CONVERSION OF URIDINE DIPHOSPHATE D-GLUCURONIC ACID TO URIDINE DIPHOSPHATE GALACTURONIC ACID, URIDINE DIPHOSPHATE XYLOSE, AND URIDINE DIPHOSPHATE ARABINOSE1,2 (1958) (43)
The iduronidase-deficient mucopolysaccharidoses: clinical and roentgenorgraphic features. (1976) (43)
A distinct biochemical deficit in the Maroteaux-Lamy syndrome (mucopolysaccharidosis VI). (1972) (42)
Effect of adenine nucleotides on reactions involving triphosphopyridine nucleotide. (1955) (42)
Metabolism of D-glucuronic acid and D-galacturonic acid by Phaseolus aureus seedlings. (1961) (41)
The relationship of α-l-iduronidase and Hurler corrective factor (1976) (40)
Short-term enzyme replacement in the murine model of Sanfilippo syndrome type B. (2000) (39)
Evidence for degradation of mRNA encoding alpha-L-iduronidase in Hurler fibroblasts with premature termination alleles. (1994) (39)
Enzyme replacement therapy (2004) (37)
Detection of hunter heterozygotes by enzymatic analysis of hair roots. (1979) (36)
Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndrome. (1977) (36)
Human kidney α-l-Iduronidase: Purification and characterization (1978) (35)
Enzymic phosphorylation of D-glucuronic acid by extracts from seedlings of Phaseolus aureus. (1959) (35)
Enzyme replacement therapy – a brief history (2006) (35)
Limited proteolysis of the beta-hexosaminidase precursor in a cell-free system. (1981) (34)
A third mutation at the CpG dinucleotide of codon 504 and a silent mutation at codon 506 of the HEX A gene. (1991) (34)
Cardiac manifestations in the mouse model of mucopolysaccharidosis I. (2005) (34)
Transfer of N-acetylneuraminic acid to incomplete glycoproteins associated with microsomes. (1966) (34)
Phosphorylation of D-galacturonic acid by extracts from germinating seeds of Phaseolus aureus. (1961) (33)
Formation and epimerization of dTDP-D-galactose catalyzed by plant enzymes. (1962) (32)
From serendipity to therapy. (2011) (32)
Synthesis and maturation of cross-reactive glycoprotein in fibroblasts deficient in arylsulfatase A activity. (1983) (32)
Proteolytic processing of the beta-subunit of the lysosomal enzyme, beta-hexosaminidase, in normal human fibroblasts. (1989) (32)
Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresis. (1970) (31)
Isolation of uridine diphosphate-galacturonic acid from seedlings of Phaseolus aureus. (1961) (31)
Four novel mutations underlying mild or intermediate forms of α‐L‐iduronidase deficiency (MPS IS and MPS IH/S) (1995) (29)
BIOSYNTHESIS OF LYSOSOMAL ENZYMES IN DIPLOID HUMAN FIBROBLASTS (1979) (28)
Overexpression of the human lysosomal enzyme alpha-L-iduronidase in Chinese hamster ovary cells. (1994) (28)
alpha-L-iduronidase forms semi-crystalline spherulites with amyloid-like properties. (2000) (27)
Xylosyl transfer catalyzed by an asparagus extract. (1959) (27)
Formation of GDP-L-galactose from GDP-D-mannose. (1967) (26)
Rhamnosyl transfer from TDPL-rhamnose catalyzed by a plant enzyme. (1961) (26)
A deletion/insertion mutation in the IDUA gene in a Libyan Jewish patient with Hurler syndrome (mucopolysaeeharidosis IH) (1993) (24)
The biochemical basis for mucopolysaccharidoses and mucolipidoses. (1974) (23)
A RAPID PROCEDURE FOR THE PREPARATION OF SMALL QUANTITIES OF URIDINE DIPHOSPHATE-N-(14C)ACETYLHEXOSAMINE. (1964) (22)
Purification and characterization of recombinant human alpha-N-acetylglucosaminidase secreted by Chinese hamster ovary cells. (2000) (22)
Iduronate sulfatase from human plasma. (1982) (22)
A radioactive substrate and assay for α-l-iduronidase (1977) (22)
Fluorescence derivatisation of urinary corticosteroids for high-performance liquid chromatographic analysis. (1998) (20)
Non-protein sulfhydryl compounds in the division of eggs of Strongylocentrotus purpuratus. (1957) (19)
Neurochemical Characterization of Canine α‐L‐Iduronidase Deficiency Disease (Model of Human Mucopolysaccharidosis I) (1985) (19)
Mutation in Scheie syndrome (MPS IS): A G→A transition creates new splice site in intron 5 of one IDUA allele (1993) (19)
p-Isothiocyanatophenyl 6-phospho-alpha-D-mannopyranoside coupled to albumin. A model compound recognized by the fibroblast lysosomal enzyme uptake system. 2. Biological properties. (1980) (19)
Normal transcription of the beta-hexosaminidase alpha-chain gene in the Ashkenazi Tay-Sachs mutation. (1988) (19)
Metabolism of sulfated mucopolysaccharide in cultured fibroblasts from cystic fibrosis patients. (1970) (19)
A shortened beta-hexosaminidase alpha-chain in an Italian patient with infantile Tay-Sachs disease. (1987) (18)
ENZYMATIC SYNTHESIS OF URIDINE DIPHOSPHATE XYLOSE AND URIDINE DIPHOSPHATE ARABINOSE. (1956) (18)
Gene Therapy for Human Genetic Disease? (1972) (16)
Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapy. (1972) (16)
Proteolytic processing of the alpha-chain of the lysosomal enzyme, beta-hexosaminidase, in normal human fibroblasts. (1988) (16)
Attempted enzyme replacement using human amnion membane implantations in mucopolysaccharidoses (1992) (15)
Nonuniform Deficiency of Hexosaminidase A in Tissues and Fluids of Two Unrelated Individuals (1982) (15)
Isolation of GDP-L-galactose from the albumen gland of Helix pomatia. (1966) (15)
Enzymic diagnosis of the genetic mucopolysaccharide storage disorders. (1978) (14)
A rapid and sensitive assay for neuraminidase: application to cultured fibroblasts. (1979) (13)
Genetic Errors of Mucopolysaccharide Degradation (1973) (12)
Studies of lysosomal enzyme biosynthesis in cultured cells. (1983) (12)
Insects as warfare agents in the Ancient Near East (Ex. 23:28; Deut. 7:20; Josh. 24:12; Isa. 7:18-20). (1980) (12)
An evaluation of three methods for the measurement of diamine oxidase (DAO) activity in amniotic fluid. (1979) (12)
Two abnormalities of hexosaminidase A in clinically normal individuals. (1986) (12)
THYMIDINE DIPHOSPHATE D-GALACTOSE PYROPHOSPHORYLASE OF PHASEOLUS AUREUS. (1963) (12)
Enzymes of Carbohydrate Synthesis (1964) (11)
Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier state. (1976) (11)
Excretion of polyamines by the pregnant rat following inhibition of diamine oxidase (1979) (11)
Defective phosphorylation and processing of beta-hexosaminidase by intact cultured fibroblasts from patients with mucolipidosis III. (1982) (11)
Separation of imidazoles in the histidine-loading test. (1968) (10)
A mutant stop codon (TAG) in the IDUA gene is used as an acceptor splice site in a patient with Hurler syndrome (MPS IH) (1994) (9)
Hydrolysis of amylose by β-amylase and Z-enzyme (1955) (9)
The Hunter syndrome in a 46 XX girl. (1973) (8)
A canine model of human a-L-iduronidase deficiency ( mucopolysaccharidosis I / Hurler-Scheie syndrome / correction / mannose 6-phosphate ) (8)
Administration of iduronate sulfatase by plasma exchange to patients with the Hunter syndrome: a clinical study. (1982) (8)
Stimulation of a protein glycosylation reaction by lysozyme. (1969) (8)
Author Correction: Lysosomal storage diseases (2018) (7)
Genetic Disorders of Mucopolysaccharide Metabolism (1973) (6)
Observations on the chemical and physiological properties of urodiolenone, an urinary compound found in hypertension. (1985) (6)
Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells. (1973) (6)
Mucopolysaccharidoses: The Biochemical Approach (1972) (6)
Lessons from genetic disorders of lysosomes. (1979) (6)
The enzymology of inherited mucopolysaccharide storage disorders (1977) (6)
The effect of L-thyroxine on histidine metabolism. (1971) (6)
DEFECTIVE SYNTHESIS OR MATURATION OF THE α-CHAIN OF β-HEXOSAMINIDASE IN CLASSIC AND VARIANT FORMS OF TAY-SACHS DISEASE (1984) (5)
Publisher Correction: Lysosomal storage diseases (2019) (5)
GENETIC COUNSELLING FOR HUNTER SYNDROME (1976) (5)
843 AMNIOTIC MEMBRANE IMPLANTATION IN MUCOPOLYSACCHARIDOSIS (1985) (5)
[46] UDP-d-galacturonic acid 4-epimerase from radish roots (1966) (5)
Hydrolysis of glycopyranosyl phosphates of the β-d (or α-l) configuration by a plant phosphatase (1962) (4)
Deficiency of Specific Proteins in the Inborn Errors of Mucopolysaccharide Metabolism (1972) (4)
14. Biosynthesis of normal and mutant β-hexosaminidases (2001) (4)
Correction: Defects in the Medial Entorhinal Cortex and Dentate Gyrus in the Mouse Model of Sanfilippo Syndrome Type B (2012) (4)
Biochemical studies in mucolipidoses II and III. (1975) (3)
Intracerebroventricular enzyme replacement therapy with glycosylation-independent lysosomal targeted NAGLU leads to widespread enzymatic activity, reduction of lysosomal storage and of secondary defects in brain of mice with Sanfilippo syndrome type B (2014) (3)
Serum urocanase as an aid in the differential diagnosis of liver disorders. (1969) (3)
Architecture of the gene encoding alpha-L-iduronidase and some mutations underlying human and canine mucopolysaccharidosis I (1992) (3)
Replacement of genotype-specific proteins in mucopolysaccharidoses. (1973) (3)
Human kidney alpha-L-iduronidase: purification and characterization. (1978) (3)
[108] Preparation of UDP-d-xylose and UDP-l-arabinose (1963) (3)
Biosynthesis of normal and mutant beta-hexosaminidases. (2001) (2)
The excretion of imidazoles following histidine loading in cases of thyrotoxicosis. (1971) (2)
Excretion of imidazole derivatives following a histidine load in pregnancy. (1971) (2)
EXCRETION OF FORMIMINOGLUTAMIC ACID AND UROCANIC ACID (1966) (2)
693. Retrovirally Transduced Bone Marrow Has Effect on Brain Pathology in Mouse Model of Mucopolysaccharidosis IIIB (2004) (1)
Effect of estrogens on histidine metabolism. (1973) (1)
A cystic fibrosis phenotype in cells cultured from sweat gland secretory coil. Altered kinetics of 36Cl efflux. (1990) (1)
THE BIOCHEMICAL BASIS OF THE INBORN ERRORS OF MUCOPOLYSACCHARIDE METABOLISM (1972) (1)
INHERITED DISORDERS OF LYSOSOMAL METABOLISM x887 (1975) (0)
The relationship of alpha-L-iduronidase and Hurler corrective factor. (1976) (0)
The Defect in the Hurler and Scheie Syndromes : Deficiency of caL-Iduronidase ( skin fibroblasts / mucopolysaccharidosis ) (0)
The William Allan Memorial Award address: cell mixing and its sequelae. (1983) (0)
Sanfi ippoSyndrome: Profound Deficiency ofAlpha-Acetylglucosaminidase Activity inOrgansandSkinFibroblasts fromType-BPatients (genetic disease/mucopolysaccharidosis/lysosomes/enzyme) (1972) (0)
Victor Ginsburg, the early years (2004) (0)
Recent studies on the maturation of lysosomal enzymes (1982) (0)
Erratum: (Mammalian Genome (1996) 7:9 (2465-2494)) (1997) (0)
THE RECEPTOR FOR LYSOSOMAL ENZYMES ON THE SURFACE OF CULTURED FIBROBLASTS (1981) (0)
Pleiotropic mutations of lysosomal function in human patients and in Chinese hamster ovary cells. (1982) (0)
TECHNICALMETHODS A RAPIDMETHOD FOR DETERMININGFAECAL FAT (1952) (0)
Cyproheptadine and Sexism (1980) (0)
Study of serum urocanase in liver diseases. (1971) (0)
CELL INTERACTION IN THE PACKAGING OF LYSOSOMAL ENZYMES (1975) (0)
Synthesis of j8-hexosaminidase in cell-free translation and in intact fibroblasts: An insoluble precursor (0)
Hydrolysis of glycopyranosyl phosphates of teh beta-D (or alpha-L) configuration by a plant phosphatase. (1962) (0)
Genetic diseases of mucopolysaccharide catabolism; single-enzyme deficiency disorders. (1977) (0)
A radioactive substrate and assay for alpha-L-iduronidase. (1977) (0)
EFFECT OF SOLVENTS AND OF TEMPERATURE ON THE OPTICAL ROTATORY PROPERTIES OF PEPSIN*4t (0)
Human , B-hexosaminidase a chain : Coding sequence and homology with the f 8 chain ( lysosomal enzyme / Tay-Sachs disease / cDNA sequencing / second mRNA / chromosomal loalization ) (0)
Co-Workers of Nils Alwall Contributing to the Festschrift (1985) (0)
Proceedings: Polyamine excretion in pregnancy. (1975) (0)
1. Evidence for two different biochemical defects causing Sanfilippo syndrome (1971) (0)
A case of unexplained excretion of urocanic acid and urocanyl glycine after a histidine loading test. (1970) (0)
Lysosomes. Cellular Organelles. Eric Holtzman (1990) (0)
Letter: Phenotypic variation in alpha-L-iduronidase deficiency. (1975) (0)
INTEGRATED MAGNETIC AND SUPERCONDUCTIVE MEMORIES (0)
Urinary urocanic acid determination: a criticism. (1972) (0)
Long-term and high dose enzyme replacement therapy in the canine mucopolysaccharidosis I model (1995) (0)
Hydrolysis of amylose by beta-amylase and Z-enzyme. (1955) (0)
Lack of inhibition of diamine oxidase during hydralazine therapy. (1984) (0)

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