William B Rizzo, MD

Professor

  • 5776 Citations
  • 34 h-Index
1977 …2019
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Research Output 1977 2019

Article
5 Citations (Scopus)

221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative

Bentler, K., Zhai, S., Elsbecker, S. A., Arnold, G. L., Burton, B. K., Vockley, J., Cameron, C. A., Hiner, S. J., Edick, M. J., Berry, S. A., Thomas, J., Dodge, M., Singh, R., Lakshman, S., Coakley, K., Stembridge, A., Russi, A. S., Phillips, E., Burton, B., Edano, C. & 62 others, Shrestha, S., Hoganson, G., Dwyer, L., Hainline, B., Romie, S., Hainline, S., Asamoah, A., Goodin, K., Rajakaruna, C., Jackson, K., Hamosh, A., Vernon, H., Smith, N., Ahmad, A., Lipinski, S., Feldman, G., Berry, S., Elsbecker, S., Bentler, K., Font-Montgomery, E., Peck, D., Pena, L. D. M., Koeberl, D. D., Jiang, Y. H., Kishnani, P. S., Rizzo, W. B., Dawson, M., Ambrose, N., Levy, P., Kronn, D., Fong, C. T., D'Aco, K., Hart, T., Erbe, R., Samons, M., Leslie, N., Powers, R., Bartholomew, D., Goff, M., vanCalcar, S., Hansen, J., Arnold, G., Vockley, J., Walsh-Vockley, C., Rhead, W., Dimmock, D., Engelking, P., Bird, C., Swan, A., Schwoerer, J. S., Henry, S., Narumanchi, T. C., Hummel, M., Wilkins, J., Davis-Keppen, L., Stein, Q., Loman, R., Cameron, C., Edick, M. J., Hiner, S. J., Justice, K. & Zhai, S., Sep 1 2016, In : Molecular Genetics and Metabolism. 119, 1-2, p. 75-82 8 p.

Research output: Contribution to journalArticle

Acyl-CoA Dehydrogenase
Inborn Errors Metabolism
Metabolism
Health
Newborn Infant
31 Citations (Scopus)

Abnormal fatty alcohol metabolism in cultured keratinocytes from patients with Sjögren-Larsson syndrome

Rizzo, W. B., Craft, D. A., Somer, T., Carney, G., Trafrova, J. & Simon, M., Feb 1 2008, In : Journal of Lipid Research. 49, 2, p. 410-419 10 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Fatty Alcohols
Keratinocytes
Metabolism
long-chain-alcohol dehydrogenase
23 Citations (Scopus)

A common deletion mutation in European patients with Sjogren-Larsson syndrome

Rizzo, W. B., Carney, G. & De Laurenzi, V., Dec 1997, In : Biochemical and Molecular Medicine. 62, 2, p. 178-181 4 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Sjogren-Larsson Syndrome
Sequence Deletion
Mutation
Exons
59 Citations (Scopus)

Adrenoleukodystrophy: Effects of dietary restriction of very long chain fatty acids and of administration of carnitine and clofibrate on clinical status and plasma fatty acids

Brown, F. R., van Duyn, M. A. S., Moser, A. B., Schulman, J. D., Rizzo, W. B., Snyder, R. D., Murphy, J. V., Kamoshita, S. & Migeon, C. J., Dec 1 1982, In : Johns Hopkins Medical Journal. 151, 4, p. 164-172 9 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Clofibrate
Carnitine
Fatty Acids
Peroxisomal Disorders
75 Citations (Scopus)

Adrenoleukodystrophy: Dietary oleic acid lowers hexacosanoate levels

Rizzo, W. B., Phillips, M. W., Dammann, A. L., Leshner, R. T., Jennings, S. S., Avigan, J. & Proud, V. K., Mar 1987, In : Annals of Neurology. 21, 3, p. 232-239 8 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Oleic Acid
Fatty Acids
Erythrocytes
Monounsaturated Fatty Acids
51 Citations (Scopus)

Adrenoleukodystrophy: Very long-chain fatty acid metabolism in fibroblasts

Rizzo, W. B., Avigan, J., Chemke, J. & Schulman, J. D., Feb 1984, In : Neurology. 34, 2, p. 163-169 7 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Fatty Acids
Fibroblasts
Palmitates
Serum
100 Citations (Scopus)

Adrenoleukodystrophy: Oleic acid lowers fibroblast saturated C22–26 fatty acids

Rizzo, W. B., Watkins, P. A., Phillips, M. W., Cranin, D., Campbell, B. & Avigan, J., Mar 1986, In : Neurology. 36, 3, p. 357-361 5 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Oleic Acid
Fatty Acids
Fibroblasts
Monounsaturated Fatty Acids
5 Citations (Scopus)

A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkers

Wangler, M. F., Hubert, L., Donti, T. R., Ventura, M. J., Miller, M. J., Braverman, N., Gawron, K., Bose, M., Moser, A. B., Jones, R. O., Rizzo, W. B., Sutton, V. R., Sun, Q., Kennedy, A. D. & Elsea, S. H., Oct 1 2018, In : Genetics in Medicine. 20, 10, p. 1274-1283 10 p.

Research output: Contribution to journalArticle

Zellweger Syndrome
Peroxisomes
Metabolomics
Biomarkers
Sphingomyelins
2 Citations (Scopus)

An immune tolerance approach using transient low-dose methotrexate in the ERT-naïve setting of patients treated with a therapeutic protein: experience in infantile-onset Pompe disease

Kazi, Z. B., Desai, A. K., Troxler, R. B., Kronn, D., Packman, S., Sabbadini, M., Rizzo, W. B., Scherer, K., Abdul-Rahman, O., Tanpaiboon, P., Nampoothiri, S., Gupta, N., Feigenbaum, A., Niyazov, D. M., Sherry, L., Segel, R., McVie-Wylie, A., Sung, C., Joseph, A. M., Richards, S. & 1 others, Kishnani, P. S., Apr 1 2019, In : Genetics in Medicine. 21, 4, p. 887-895 9 p.

Research output: Contribution to journalArticle

Glycogen Storage Disease Type II
Immune Tolerance
Methotrexate
Proteins
Therapeutics
16 Citations (Scopus)

Attitudes toward presymptomatic testing and prenatal diagnosis for adrenoleukodystrophy among affected families

Costakos, D., Abramson, R. K., Edwards, J. G., Rizzo, W. B. & Best, R. G., Jan 1 1991, In : American journal of medical genetics. 41, 3, p. 295-300 6 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Prenatal Diagnosis
X-Linked Genes
Nuclear Family
Fetus
6 Citations (Scopus)

A Turkish family with Sjögren-Larsson syndrome caused by a novel ALDH3A2 mutation

Incecik, F., Herguner, O. M., Rizzo, W. B. & Altunbasak, S., Jul 1 2013, In : Annals of Indian Academy of Neurology. 16, 3, p. 425-427 3 p.

Research output: Contribution to journalArticle

varespladib methyl
long-chain-aldehyde dehydrogenase
Mutation
Neurocutaneous Syndromes
Ichthyosis
20 Citations (Scopus)

Carrier detection for Sjögren-Larsson syndrome

Kelson, T. L., Craft, D. A. & Rizzo, W. B., Jan 1 1992, In : Journal of Inherited Metabolic Disease. 15, 1, p. 105-111 7 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Heterozygote
long-chain-alcohol dehydrogenase
Fibroblasts
Homozygote
29 Citations (Scopus)

Changes in phosphatidylcholine fatty acid composition are associated with altered skeletal muscle insulin responsiveness in normal man

Clore, J. N., Harris, P. A., Li, J., Azzam, A., Gill, R., Zuelzer, W., Rizzo, W. B. & Blackard, W. G., Jan 1 2000, In : Metabolism: Clinical and Experimental. 49, 2, p. 232-238 7 p.

Research output: Contribution to journalArticle

Phosphatidylcholines
Skeletal Muscle
Fatty Acids
Niacin
Insulin
29 Citations (Scopus)

Clinical variation in X-linked adrenoleukodystrophy: Fatty acid and lipid metabolism in cultured fibroblasts

Boles, D. J., Craft, D. A., Padgett, D. A., Loria, R. M. & Rizzo, W. B., Feb 1991, In : Biochemical Medicine and Metabolic Biology. 45, 1, p. 74-91 18 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Fibroblasts
Lipid Metabolism
Fatty Acids
Palmitates
222 Citations (Scopus)

Cysteamine Therapy for Children with Nephropathic Cystinosis

Gahl, W. A., Reed, G. F., Thoene, J. G., Schulman, J. D., Rizzo, W. B., Jonas, A. J., Denman, D. W., Schlesselman, J. J., Corden, B. J. & Schneider, J. A., Apr 16 1987, In : New England Journal of Medicine. 316, 16, p. 971-977 7 p.

Research output: Contribution to journalArticle

Cystinosis
Cysteamine
Cystine
Control Groups
Therapeutics
17 Citations (Scopus)

Diagnosis of inborn errors of phytanic acid oxidation using tritiated phytanic acid.

Zenger-Hain, J., Craft, D. A. & Rizzo, W. B., 1992, In : Progress in clinical and biological research. 375, p. 399-407 9 p.

Research output: Contribution to journalArticle

Phytanic Acid
Inborn Errors Metabolism
Tritium
Solubility
Oxidation-Reduction
155 Citations (Scopus)

Dietary erucic acid therapy for X-linked adrenoleukodystrophy

Rizzo, W. B., Leshner, R. T., Odone, A., Dammann, A. L., Craft, D. A., Jensen, M. E., Jennings, S. S., Davis, S., Jaitly, R. & Sgro, J. A., Nov 1989, In : Neurology. 39, 11, p. 1415-1422 8 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Oleic Acid
Diet
Therapeutics
Leukoencephalopathies
6 Citations (Scopus)

Dietary fatty acids temporarily alter liver very long-chain fatty acid composition in mice

Boles, D. J. & Rizzo, W. B., Jan 1 1992, In : Journal of Nutrition. 122, 8, p. 1662-1671 10 p.

Research output: Contribution to journalArticle

very long chain fatty acids
dietary fat
Fatty Acids
fatty acid composition
liver
3 Citations (Scopus)

Dolichol kinase deficiency (DOLK-CDG): Two new cases and expansion of phenotype

Rush, E. T., Baker, C. V. & Rizzo, W. B., Sep 2017, In : American Journal of Medical Genetics, Part A. 173, 9, p. 2428-2434 7 p.

Research output: Contribution to journalArticle

Congenital Disorders of Glycosylation
dolichol kinase
Phenotype
Oligosaccharides
Mutation
12 Citations (Scopus)

Dyggve-Melchior-Clausen syndrome with increased pipecolic acid in plasma and urine

Roesel, R. A., Carroll, J. E., Rizzo, W. B., van der Zalm, T. & Hahn, D. A., Nov 1 1991, In : Journal of Inherited Metabolic Disease. 14, 6, p. 876-880 5 p.

Research output: Contribution to journalArticle

Phytanic Acid
Plasmalogens
Fatty Acids
Urine
pipecolic acid
24 Citations (Scopus)

Effect of biotin deficiency and supplementation on lipid metabolism in rats, saturated fatty acids

Suchy, S. F., Rizzo, W. B. & Wolf, B., Jan 1 1986, In : American Journal of Clinical Nutrition. 44, 4, p. 475-480 6 p.

Research output: Contribution to journalArticle

biotin
Lipid Metabolism
lipid metabolism
saturated fatty acids
Fatty Acids
7 Citations (Scopus)

Effects of fructose and troglitazone on phospholipid fatty acid composition in rat skeletal muscle

Clore, J. N., Li, J. & Rizzo, W. B., Jan 1 2000, In : Lipids. 35, 11, p. 1281-1287 7 p.

Research output: Contribution to journalArticle

troglitazone
Fructose
Muscle
Rats
Phospholipids
1 Citation (Scopus)

Emotional experience in parents of children with Zellweger spectrum disorders: A qualitative study

Bose, M., Mahadevan, M., Schules, D. R., Coleman, R. K., Gawron, K. M., Gamble, M. B., Roullet, J. B., Gibson, K. M. & Rizzo, W. B., Jun 2019, In : Molecular Genetics and Metabolism Reports. 19, 100459.

Research output: Contribution to journalArticle

Open Access
Zellweger Syndrome
Parents
Caregivers
Focus Groups
Emotions
17 Citations (Scopus)

Fatty acid alterations and carboxylase deficiencies in the skin of biotin-deficient rats

Proud, V. K., Rizzo, W. B., Patterson, J. W., Heard, G. S. & Wolf, B., May 1990, In : American Journal of Clinical Nutrition. 51, 5, p. 853-858 6 p.

Research output: Contribution to journalArticle

biotin
Biotin
skin (animal)
Fatty Acids
fatty acids

Fatty Acids in Biotin Deficiency

SUCHY, SHARON. F., RIZZO, WILLIAM. B. & WOLF, BARRY., Jun 1985, In : Annals of the New York Academy of Sciences. 447, 1, p. 429 1 p.

Research output: Contribution to journalArticle

Fatty Acids
Biotin deficiency
18 Citations (Scopus)

Fatty Alcohol Accumulation in the Autosomal Recessive Form of Rhizomelic Chondrodysplasia Punctata

Rizzo, W. B., Craft, D. A., Judd, L. L., Moser, H. W. & Moser, A. B., Aug 1 1993, In : Biochemical Medicine and Metabolic Biology. 50, 1, p. 93-102 10 p.

Research output: Contribution to journalArticle

Rhizomelic Chondrodysplasia Punctata
Fatty Alcohols
Peroxisomal Disorders
Palmitates
Fibroblasts
63 Citations (Scopus)

Fatty alcohol metabolism in cultured human fibroblasts. Evidence for a fatty alcohol cycle

Rizzo, W. B., Craft, D. A., Dammann, A. L. & Phillips, M. W., Dec 1 1987, In : Journal of Biological Chemistry. 262, 36, p. 17412-17419 8 p.

Research output: Contribution to journalArticle

Fatty Alcohols
Palmitates
Fibroblasts
Metabolism
Palmitic Acid
24 Citations (Scopus)

Fatty aldehyde dehydrogenase: Genomic structure, expression and mutation analysis in Sjögren-Larsson syndrome

Rizzo, W. B., Lin, Z. & Carney, G., Jan 30 2001, In : Chemico-Biological Interactions. 130-132, p. 297-307 11 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Mutation
Genes
Phytanic Acid
Fatty Alcohols
24 Citations (Scopus)

Genetic homogeneity in Sjogren-Larsson syndrome: Linkage to chromosome 17p in families of different non-Swedish ethnic origins

Rogers, G. R., Rizzo, W. B., Zlotogorski, A., Hashem, N., Lee, M., Compton, J. G. & Bale, S. J., Jan 1 1995, In : American Journal of Human Genetics. 57, 5, p. 1123-1129 7 p.

Research output: Contribution to journalArticle

Sjogren-Larsson Syndrome
Chromosomes
Chromosomes, Human, Pair 17
Genes
Ichthyosis
14 Citations (Scopus)

Genetics and prospective therapeutic targets for Sjögren-Larsson Syndrome

Rizzo, W. B., Apr 2 2016, In : Expert Opinion on Orphan Drugs. 4, 4, p. 395-406 12 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Aldehydes
Peroxisome Proliferator-Activated Receptors
Farnesol
Ichthyosis
20 Citations (Scopus)

Genomic organization, expression, and alternate splicing of the mouse fatty aldehyde dehydrogenase gene

Lin, Z., Carney, G. & Rizzo, W. B., Jan 1 2000, In : Molecular Genetics and Metabolism. 71, 3, p. 496-505 10 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Alternative Splicing
Genes
Exons
Sjogren-Larsson Syndrome
49 Citations (Scopus)

Genomic organization and expression of the human fatty aldehyde dehydrogenase gene (FALDH)

Rogers, G. R., Markova, N. G., De Laurenzi, V., Rizzo, W. B. & Compton, J. G., Jan 15 1997, In : Genomics. 39, 2, p. 127-135 9 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Sjogren-Larsson Syndrome
Genes
Exons
Transcription Initiation Site
4 Citations (Scopus)

Genotype and phenotype variability in Sjögren-Larsson syndrome

Weustenfeld, M., Eidelpes, R., Schmuth, M., Rizzo, W. B., Zschocke, J. & Keller, M. A., Feb 1 2019, In : Human mutation. 40, 2, p. 177-186 10 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Genotype
Phenotype
Ichthyosis
Poisons
98 Citations (Scopus)

Human liver fatty aldehyde dehydrogenase: Microsomal localization, purification, and biochemical characterization

Kelson, T. L., Secor McVoy, J. R. & Rizzo, W. B., Apr 17 1997, In : Biochimica et Biophysica Acta - General Subjects. 1335, 1-2, p. 99-110 12 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Liver
Purification
Sjogren-Larsson Syndrome
2-butenal
21 Citations (Scopus)

Ichthyosis, Mental Retardation, and Asymptomatic Spasticity: A New Neurocutaneous Syndrome with Normal Fatty Alcohol:NAD+ Oxidoreductase Activity

Koone, M. D., Rizzo, W. B., Elias, P. M., Williams, M. L., Lightner, V. & Pinnell, S. R., Nov 1990, In : Archives of Dermatology. 126, 11, p. 1485-1490 6 p.

Research output: Contribution to journalArticle

long-chain-alcohol dehydrogenase
Neurocutaneous Syndromes
Fatty Alcohols
Ichthyosis
Lipid Metabolism
33 Citations (Scopus)

Ichthyosis in Sjögren-Larsson syndrome reflects defective barrier function due to abnormal lamellar body structure and secretion

Rizzo, W. B., S'Aulis, D., Jennings, M. A., Crumrine, D. A., Williams, M. L. & Elias, P. M., Aug 1 2010, In : Archives of Dermatological Research. 302, 6, p. 443-451 9 p.

Research output: Contribution to journalArticle

Ichthyosis
Cornea
long-chain-aldehyde dehydrogenase
Membranes
Skin Abnormalities
24 Citations (Scopus)

Identification of new markers in Xp21 between DXS28 (C7) and DMD

Worley, K. C., Towbin, J. A., Zhu, X. M., Barker, D. F., Ballabio, A., Chamberlain, J., Biesecker, L. G., Blethen, S. L., Brosnan, P., Fox, J. E., Rizzo, W. B., Romeo, G., Sakuragawa, N., Seltzer, W. K., Yamaguchi, S. & McCabe, E. R. B., Aug 1992, In : Genomics. 13, 4, p. 957-961 5 p.

Research output: Contribution to journalArticle

Sequence Tagged Sites
Duchenne Muscular Dystrophy
Clone Cells
Yeast Artificial Chromosomes
Multiplex Polymerase Chain Reaction
16 Citations (Scopus)

Immunological probes for chromatin structure

Bustin, M., Kurth, P. D., Moudrianakis, E. N., Goldblatt, D., Sperling, R. & Rizzo, W. B., Dec 1 1977, In : Cold Spring Harbor Symposia on Quantitative Biology. 42, 1, p. 379-388 10 p.

Research output: Contribution to journalArticle

histones
Histones
Chromatin
chromatin
Chromosomes
5 Citations (Scopus)

Induction, titration, and maintenance dosing regimen in a phase 2 study of pegvaliase for control of blood phenylalanine in adults with phenylketonuria

Zori, R., Thomas, J. A., Shur, N., Rizzo, W. B., Decker, C., Rosen, O., Li, M., Schweighardt, B., Larimore, K. & Longo, N., Nov 2018, In : Molecular Genetics and Metabolism. 125, 3, p. 217-227 11 p.

Research output: Contribution to journalArticle

Phenylketonurias
Phenylalanine
Titration
Blood
Maintenance
27 Citations (Scopus)

Inherited disorders of fatty alcohol metabolism

Rizzo, W. B., Oct 1998, In : Molecular Genetics and Metabolism. 65, 2, p. 63-73 11 p.

Research output: Contribution to journalArticle

Fatty Alcohols
Metabolism
Peroxisomal Disorders
Ether
Infantile Refsum's Disease
3 Citations (Scopus)

Intrathecal Baclofen Therapy for the Treatment of Spasticity in Sjögren-Larsson Syndrome

Hidalgo, E. T., Orillac, C., Hersh, A., Harter, D. H., Rizzo, W. B. & Weiner, H. L., Jan 1 2017, In : Journal of Child Neurology. 32, 1, p. 100-103 4 p.

Research output: Contribution to journalArticle

Baclofen
Therapeutics
Therapeutic Uses
Caregivers
Parents
55 Citations (Scopus)

Involvement of microsomal fatty aldehyde dehydrogenase in the α- oxidation of phytanic acid

Verhoeven, N. M., Jakobs, C., Carney, G., Somers, M. P., Wanders, R. J. A. & Rizzo, W. B., Jun 16 1998, In : FEBS Letters. 429, 3, p. 225-228 4 p.

Research output: Contribution to journalArticle

long-chain-aldehyde dehydrogenase
Sjogren-Larsson Syndrome
Phytanic Acid
Oxidation
Ethanolamine
10 Citations (Scopus)
Open Access
long-chain-alcohol dehydrogenase
Fatty Alcohols
Cricetulus
Ovary
Cell Line
29 Citations (Scopus)

Isolation of a Chinese hamster fibroblast variant defective in dihydroxyacetonephosphate acyltransferase activity and plasmalogen biosynthesis: Use of a novel two-step selection protocol

Nagan, N., Hajra, A. K., Larkins, L. K., Lazarow, P., Purdue, P. E., Rizzo, W. B. & Zoeller, R. A., May 15 1998, In : Biochemical Journal. 332, 1, p. 273-279 7 p.

Research output: Contribution to journalArticle

glycerone-phosphate O-acyltransferase
Plasmalogens
Biosynthesis
Fibroblasts
Cricetulus
13 Citations (Scopus)

Large contiguous gene deletions in Sjögren-Larsson syndrome

Engelstad, H., Carney, G., S'Aulis, D., Rise, J., Sanger, W. G., Rudd, M. K., Richard, G., Carr, C. W., Abdul-Rahman, O. A. & Rizzo, W. B., Nov 1 2011, In : Molecular Genetics and Metabolism. 104, 3, p. 356-361 6 p.

Research output: Contribution to journalArticle

Gene Deletion
Genes
long-chain-aldehyde dehydrogenase
Missense Mutation
Microarrays
41 Citations (Scopus)

Lectins as probes of chromatin structure. Binding of concanavalin A to purified rat liver chromatin

Rizzo, W. B. & Bustin, M., Dec 1 1977, In : Journal of Biological Chemistry. 252, 20, p. 7062-7067 6 p.

Research output: Contribution to journalArticle

Concanavalin A
Lectins
Liver
Chromatin
Rats
691 Citations (Scopus)

Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy

Biffi, A., Montini, E., Lorioli, L., Cesani, M., Fumagalli, F., Plati, T., Baldoli, C., Martino, S., Calabria, A., Canale, S., Benedicenti, F., Vallanti, G., Biasco, L., Leo, S., Kabbara, N., Zanetti, G., Rizzo, W. B., Mehta, N. A. L., Cicalese, M. P., Casiraghi, M. & 17 others, Boelens, J. J., Del Carro, U., Dow, D. J., Schmidt, M., Assanelli, A., Neduva, V., Di Serio, C., Stupka, E., Gardner, J., Von Kalle, C., Bordignon, C., Ciceri, F., Rovelli, A., Roncarolo, M. G., Aiuti, A., Sessa, M. & Naldini, L., Jan 1 2013, In : Science. 341, 6148, 1233158.

Research output: Contribution to journalArticle

Metachromatic Leukodystrophy
Cell- and Tissue-Based Therapy
Hematopoietic Stem Cells
Genetic Therapy
Cerebroside-Sulfatase
13 Citations (Scopus)

Liposome-mediated transfer of simian virus 40 DNA and minichromosome into mammalian cells

Rizzo, W. B., Schulman, J. D. & Mukherjee, A. B., Jan 1 1983, In : Journal of General Virology. 64, 4, p. 911-919 9 p.

Research output: Contribution to journalArticle

Open Access
Simian virus 40
Liposomes
DNA
Deoxyribonucleases
Salmon
7 Citations (Scopus)

Low bone mineral density is a common feature of Zellweger spectrum disorders

Rush, E. T., Goodwin, J. L., Braverman, N. E. & Rizzo, W. B., Jan 1 2016, In : Molecular Genetics and Metabolism. 117, 1, p. 33-37 5 p.

Research output: Contribution to journalArticle

Zellweger Syndrome
Bone Density
Minerals
Bone
Bone Diseases
1 Citation (Scopus)

Meeting report from frontiers in ichthyosis research

Milstone, L. M., Rizzo, W. B. & Pickford, J. R., Feb 1 2011, In : Journal of Investigative Dermatology. 131, 2, p. 279-282 4 p.

Research output: Contribution to journalArticle

International cooperation