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Growth Plate Pathology in the Mucopolysaccharidosis Type VI Rat Model—An Experimental and Computational Approach
 
 
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Correction

Correction: Barak, S. et al. “Long-Term Outcomes of Early Enzyme Replacement Therapy for Mucopolysaccharidosis IV: Clinical Case Studies of Two Siblings”. Diagnostics 2020, 10, 108

1
Department of Pediatric Rehabilitation, Edmond and Lily Safra Children’s Hospital, Chaim Sheba Medical Center, Ramat-Gan 5265601, Israel
2
Kaye Academic College of Education, M.Ed. Programs, Beer-Sheva 8414201, Israel
3
The Sackler School of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel
4
Edmond and Lily Safra Children’s Hospital, Chaim Sheba Medical Center, Ramat Gan 5265601, Israel
5
Wohl Institute for Translational Medicine, Chaim Sheba Medical Center, Ramat Gan 5265601, Israel
6
The National AT Center, Chaim Sheba Medical Center, Ramat Gan 5265601, Israel
7
The Pediatric Pulmonology Unit, Chaim Sheba Medical Center, Edmond and Lilly Safra Children Hospital, Tel HaShomer, Ramat Gan 5265601, Israel
8
Pediatric Endocrine and Diabetes Unit, Chaim Sheba Medical Center, Edmond and Lily Safra Children’s Hospital, Ramat-Gan 5265601, Israel
9
Pediatric Orthopedic Unit, Edmond and Lilly Safra Children Hospital, Chaim Sheba Medical Center, Ramat Gan 5265601, Israel
10
Institute of Rare Diseases, Edmond and Lily Safra Children’s hospital, Chaim Sheba Medical Center, Ramat Gan 5265601, Israel
11
The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv postcode Israel, Ramat Aviv 69978, Israel
*
Author to whom correspondence should be addressed.
Published: 14 July 2020
(This article belongs to the Special Issue Mucopolysaccharidoses: Diagnosis, Treatment, and Management)
The authors wish to make the following correction to this paper [1]:
In the first paragraph of the Results section: “P1 and P2 started ERT with elosulfase alfa (VIMIZIM® by BioMarin©) 5 months post-diagnosis at age 4.5 years and 11 months, respectively, with an intravenous dose of 1.0 mg/kg/week.” The value of the dose is 1.0 mg/kg/week but should be corrected to 2.0 mg/kg/week.
These changes have no material impact on the conclusions of our paper. We apologize to our readers.

Reference

  1. Barak, S.; Anikster, Y.; Sarouk, I.; Stern, E.; Eisenstein, E.; Yissar, T.; Sherr-Lurie, N.; Raas-Rothschild, A.R.; Guttman, D. Long-Term Outcomes of Early Enzyme Replacement Therapy for Mucopolysaccharidosis IV: Clinical Case Studies of Two Siblings. Diagnostics 2020, 10, 108. [Google Scholar] [CrossRef] [PubMed] [Green Version]

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MDPI and ACS Style

Barak, S.; Anikster, Y.; Sarouk, I.; Stern, E.; Eisenstein, E.; Yissar, T.; Sherr-Lurie, N.; Raas-Rothschild, A.; Guttman, D. Correction: Barak, S. et al. “Long-Term Outcomes of Early Enzyme Replacement Therapy for Mucopolysaccharidosis IV: Clinical Case Studies of Two Siblings”. Diagnostics 2020, 10, 108. Diagnostics 2020, 10, 480. https://0-doi-org.brum.beds.ac.uk/10.3390/diagnostics10070480

AMA Style

Barak S, Anikster Y, Sarouk I, Stern E, Eisenstein E, Yissar T, Sherr-Lurie N, Raas-Rothschild A, Guttman D. Correction: Barak, S. et al. “Long-Term Outcomes of Early Enzyme Replacement Therapy for Mucopolysaccharidosis IV: Clinical Case Studies of Two Siblings”. Diagnostics 2020, 10, 108. Diagnostics. 2020; 10(7):480. https://0-doi-org.brum.beds.ac.uk/10.3390/diagnostics10070480

Chicago/Turabian Style

Barak, Sharon, Yair Anikster, Ifat Sarouk, Eve Stern, Etzyona Eisenstein, Tamar Yissar, Nir Sherr-Lurie, Annick Raas-Rothschild, and Dafna Guttman. 2020. "Correction: Barak, S. et al. “Long-Term Outcomes of Early Enzyme Replacement Therapy for Mucopolysaccharidosis IV: Clinical Case Studies of Two Siblings”. Diagnostics 2020, 10, 108" Diagnostics 10, no. 7: 480. https://0-doi-org.brum.beds.ac.uk/10.3390/diagnostics10070480

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