Joel Charrow

  • 6474 Citations
1978 …2019
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Research Output 1978 2019

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Letter
2019

Addendum to Letter to the Editor: Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1

Mistry, P. K., Balwani, M., Baris, H. N., Turkia, H. B., Burrow, T. A., Charrow, J., Cox, G. F., Danda, S., Dragosky, M., Drelichman, G., El-Beshlawy, A., Fraga, C., Freisens, S., Gaemers, S., Hadjiev, E., Kishnani, P. S., Lukina, E., Maison-Blanche, P., Martins, A. M., Pastores, G. & 6 others, Petakov, M., Peterschmitt, M. J., Rosenbaum, H., Rosenbloom, B., Underhill, L. H. & Cox, T. M., Jul 1 2019, In : Blood Cells, Molecules, and Diseases. 77, p. 101-102 2 p.

Research output: Contribution to journalLetter

Gaucher Disease
Safety
Therapeutics
eliglustat
2018
2 Citations (Scopus)

Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1

Mistry, P. K., Balwani, M., Baris, H. N., Turkia, H. B., Burrow, T. A., Charrow, J., Cox, G. F., Danda, S., Dragosky, M., Drelichman, G., El-Beshlawy, A., Fraga, C., Freisens, S., Gaemers, S., Hadjiev, E., Kishnani, P. S., Lukina, E., Maison-Blanche, P., Martins, A. M., Pastores, G. & 6 others, Petakov, M., Peterschmitt, M. J., Rosenbaum, H., Rosenbloom, B., Underhill, L. H. & Cox, T. M., Jul 1 2018, In : Blood Cells, Molecules, and Diseases. 71, p. 71-74 4 p.

Research output: Contribution to journalLetter

Gaucher Disease
Safety
Therapeutics
eliglustat
2014
13 Citations (Scopus)

Gender as a disease modifier in neurofibromatosis type 1 optic pathway glioma

Fisher, M. J., Loguidice, M., Gutmann, D. H., Listernick, R. H., Ferner, R. E., Ullrich, N. J., Packer, R. J., Tabori, U., Hoffman, R. O., Ardern-Holmes, S. L., Hummel, T. R., Hargrave, D. R., Bouffet, E., Charrow, J., Bilaniuk, L. T., Balcer, L. J., D'Agostino McGowan, L. & Liu, G. T., Jan 1 2014, In : Annals of Neurology. 75, 5, p. 799-800 2 p.

Research output: Contribution to journalLetter

Optic Nerve Glioma
Neurofibromatosis 1
Learning Disorders
Vision Disorders
2008
12 Citations (Scopus)

Prevalence of type 1 Gaucher disease in the United States

Weinreb, N. J., Andersson, H. C., Banikazemi, M., Barranger, J., Beutler, E., Charrow, J., Grabowski, G. A., Hollak, C. E. M., Kaplan, P., Mankin, H., Mistry, P. K., Rosenbloom, B. E., Vom Dahl, S. & Zimran, A., Feb 11 2008, In : Archives of Internal Medicine. 168, 3, p. 326-327 2 p.

Research output: Contribution to journalLetter

2007

Response to Cohen [3]

Charrow, J., Dulisse, B., Grabowski, G. A. & Weinreb, N. J., Aug 1 2007, In : Clinical Genetics. 72, 2, 1 p.

Research output: Contribution to journalLetter

2005
10 Citations (Scopus)

The genetics of tethered cord syndrome [3]

Bassuk, A. G., Charrow, J., Gulbu, U., Epstein, L. G., Craig, D., Stephan, D. A., Jalali, A., Mukhopadhyay, A., Kessler, J. A., Kim, F., Bowman, R., Mclone, D., Yagi, H. & Matsuoka, R., Feb 1 2005, In : American Journal of Medical Genetics. 132 A, 4, p. 450-453 4 p.

Research output: Contribution to journalLetter

Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 21
Spinal Dysraphism
Neural Tube Defects
Chromosome Aberrations
2001
10 Citations (Scopus)

Comments on neurofibromatosis 1 and optic pathway tumors [1]

Listernick, R. H., Charrow, J. & Gutmann, D. H., Jul 22 2001, In : American Journal of Medical Genetics. 102, 1, 1 p.

Research output: Contribution to journalLetter

Optic Nerve Neoplasms
Neurofibromatosis 1
Glioma
Visual Acuity
Magnetic Resonance Imaging
1999
8 Citations (Scopus)

Gaucher disease [1] (multiple letters)

Beutler, E., Charrow, J., Esplin, J. A., Kaplan, P., Kolodny, E. H., Pastores, G. M., Scott, C. R., Wappner, R. S., Weinreb, N. J. & Wisch, J. S., Apr 26 1999, In : Archives of Internal Medicine. 159, 8, p. 881-882 2 p.

Research output: Contribution to journalLetter

Population Surveillance
Gaucher Disease
Disease Progression
Differential Diagnosis
7 Citations (Scopus)

Recommendations for diagnosis, evaluation, and monitoring of patients with Gaucher disease [2] (multiple letters)

Elstein, D., Abrahamov, A., Hadas-Halpern, I., Zimran, A., Charrow, J., Esplin, J. A., Kaplan, P., Kolodny, E. H., Pastores, G. M., Scott, C. R., Wappner, R. S., Weinreb, N. J. & Wisch, J. S., Jun 14 1999, In : Archives of Internal Medicine. 159, 11, p. 1254-1255 2 p.

Research output: Contribution to journalLetter

International Cooperation
Gaucher Disease
X Ray Computed Tomography
Metabolic Bone Diseases
Photon Absorptiometry
1996

Precocious puberty, growth hormone deficiency, and neurofibromatosis [5]

Vassilopoulou-Sellin, R., Habiby, R., Silverman, B., Listernick, R. & Charrow, J., Jan 1 1996, In : Journal of Pediatrics. 128, 1, 1 p.

Research output: Contribution to journalLetter

1994

In Reply

Tanz, R. R. & Charrow, J., Jan 1 1994, In : Archives of Pediatrics & Adolescent Medicine. 148, 3, 1 p.

Research output: Contribution to journalLetter

1993

Reply

Listernick, R. H. & Charrow, J., Jan 1 1993, In : The Journal of pediatrics. 122, 5, p. 834-835 2 p.

Research output: Contribution to journalLetter

1990

Abnormal test results? (I: Reply)

Charrow, J. & Hedges, L. V., Jan 1 1990, In : American Journal of Diseases of Children. 144, 10, 1 p.

Research output: Contribution to journalLetter

In Reply

Charrow, J. & Hedges, L. V., Jan 1 1990, In : American Journal of Diseases of Children. 144, 10, 1 p.

Research output: Contribution to journalLetter

1984

Reply

Paller, A., Esterly, N. B., Charrow, J. & Cahan, F. M., Jan 1 1984, In : The Journal of Pediatrics. 104, 3, 1 p.

Research output: Contribution to journalLetter

1981
1 Citation (Scopus)

Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1.

Cohen, M. M., Charrow, J. & Nadler, H. L., Jul 1 1981, In : American Journal of Human Genetics. 33, 4, p. 649-650 2 p.

Research output: Contribution to journalLetter

Orofaciodigital Syndromes
Sex Chromosome Aberrations
Multiple Abnormalities
Genetic Counseling
Prenatal Diagnosis