Works about GAUCHER'S disease treatment

Results: 116

Newborn Screening for Gaucher Disease: The New Jersey Experience.

Published in:

International Journal of Neonatal Screening (IJNS), 2025, v. 11, n. 2, p. 34, doi. 10.3390/ijns11020034

By:

Menello, Caitlin;
Pressley, Shaney;
Steffensen, Madeline;
Schmidt, Sarah;
Pedro, Helio;
Jethva, Reena;
Valdez-Gonzalez, Karen;
Adams, Darius J.;
Gupta, Punita;
King, Lorien Tambini;
Velinov, Milen;
Anderson, Sharon;
Bizargity, Peyman;
Pletcher, Beth;
Tuite, Allysa;
Kresge, Christina;
Day-Salvatore, Debra Lynn;
Kuehl, Ryan;
Ficicioglu, Can

Publication type:

Article

Terapia de reemplazo enzimático en una paciente con enfermedad de Gaucher tipo III.

Published in:

Acta Pediatrica de Mexico, 2012, v. 33, n. 1, p. 9

By:

Carbajal-Rodríguez, Luis;
Gómez-González, Fernanda;
Rodríguez-Herrera, Raymundo;
Zarco-Román, Jorge;
Mora-Tiscareño, Antonieta

Publication type:

Article

The Spectrum of Neurological Manifestations Associated with Gaucher Disease.

Published in:

Diseases, 2017, v. 5, n. 1, p. 10, doi. 10.3390/diseases5010010

By:

Lal, Tamanna Roshan;
Sidransky, Ellen

Publication type:

Article

Therapeutic potential of resveratrol for the treatment of type III Gaucher disease.

Published in:

Neurology Asia, 2015, v. 20, n. 1, p. 43

By:

Soojin Yoo;
June-Bum Kim

Publication type:

Article

EMEA approves OGS drug rejected by FDA.

Published in:

Nature Biotechnology, 2002, v. 20, n. 9, p. 858, doi. 10.1038/nbt0902-858

By:

Mitchell, Peter

Publication type:

Article

Abundant Hepatic Gaucher-Like Cells Following Chemotherapy and Bone Marrow Transplantation for Hematologic Malignancy: Report of Two Cases.

Published in:

International Journal of Surgical Pathology, 2013, v. 21, n. 1, p. 89, doi. 10.1177/1066896912456081

By:

Stenzel, Peter;
Weeks, Douglas A

Publication type:

Article

Velaglucerase alfa.

Published in:: Australian Prescriber, 2012, v. 35, n. 6, p. 210
Publication type:: Article

Small Bowel Mucosal Involvement and Mesenteric Mass Formation in a Young Female with Type 3 Gaucher Disease. A.

Published in:

2018

By:

Emanuel, Anthony J.;
Holman, Nathan;
Presnell, Susan E.;
Welsh, Cynthia T.;
Pai, Shashidhar;
Sun, Shaoli

Publication type:

Case Study

Combined miglustat and enzyme replacement therapy in two patients with type 1 Gaucher disease: two case reports.

Published in:

2018

By:

Amato, Dominick;
Patterson, Mary Anne

Publication type:

journal article

Glycosylation and functionality of recombinant ß-glucocerebrosidase from various production systems.

Published in:

Bioscience Reports, 2013, v. 33, n. 5, p. 771, doi. 10.1042/BSR20130081

By:

TEKOAH, Yoram;
TZABAN, Salit;
KIZHNER, Tali;
HAINRICHSON, Mariana;
GANTMAN, Anna;
GOLEMBO, Myriam;
AVIEZER, David;
SHAALTIEL, Yoseph

Publication type:

Article

Quality of life assessment in adults with type 1 Gaucher disease.

Published in:

1999

By:

Masek, Bruce J.;
Sims, Katherine B.;
Bove, Catherine M.;
Korson, Mark S.;
Short, Priscilla;
Norman, Dennis K.;
Masek, B J;
Sims, K B;
Bove, C M;
Korson, M S;
Short, P;
Norman, D K

Publication type:

journal article

VPRIV.

Published in:: Formulary, 2010, v. 45, n. 4, p. 113
Publication type:: Article

Successful mobilization with plerixafor and autologous hematopoietic SCT in a patient with refractory Hodgkin's lymphoma and Gaucher disease.

Published in:

2011

By:

Symeonidis, A.;
Liga, M.;
Triantafyllou, E.;
Kouraklis, A.;
Tiniakou, M.;
Karakantza, M.;
Spyridonidis, A.;
Zoumbos, N.

Publication type:

Letter

Enfermedad neuropática de Gaucher tratada con terapia de reemplazo a largo plazo.

Published in:

Revista Medica del IMSS, 2013, v. 51, n. 3, p. 340

By:

Correa, Cecilia

Publication type:

Article

Investigations on therapeutic glucocerebrosidases through paired detection with fluorescent activity-based probes.

Published in:

PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0170268

By:

Kallemeijn, Wouter W.;
Scheij, Saskia;
Hoogendoorn, Sascha;
Witte, Martin D.;
Herrera Moro Chao, Daniela;
van Roomen, Cindy P. A. A.;
Ottenhoff, Roelof;
Overkleeft, Herman S.;
Boot, Rolf G.;
Aerts, Johannes M. F. G.

Publication type:

Article

Time of Initiating Enzyme Replacement Therapy Affects Immune Abnormalities and Disease Severity in Patients with Gaucher Disease.

Published in:

PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0168135

By:

Limgala, Renuka Pudi;
Ioanou, Chidima;
Plassmeyer, Matthew;
Ryherd, Mark;
Kozhaya, Lina;
Austin, Lauren;
Abidoglu, Cem;
Unutmaz, Derya;
Alpan, Oral;
Goker-Alpan, Ozlem

Publication type:

Article

α-Synuclein accumulation and GBA deficiency due to L444P GBA mutation contributes to MPTP-induced parkinsonism.

Published in:

Molecular Neurodegeneration, 2018, v. 12, p. 1, doi. 10.1186/s13024-017-0233-5

By:

Yun, Seung Pil;
Kim, Donghoon;
Kim, Sangjune;
Kim, SangMin;
Karuppagounder, Senthilkumar S.;
Kwon, Seung-Hwan;
Lee, Saebom;
Kam, Tae-In;
Lee, Suhyun;
Ham, Sangwoo;
Park, Jae Hong;
Dawson, Valina L.;
Dawson, Ted M.;
Lee, Yunjong;
Ko, Han Seok

Publication type:

Article

QUALITY OF LIFE OF PATIENTS WITH GAUCHER DISEASE.

Published in:

Journal of Nursing UFPE / Revista de Enfermagem UFPE, 2017, v. 11, n. 11, p. 4282, doi. 10.5205/reuol.23542-49901-1-ED.1111201702

By:

de Oliveira Freitas, Saulo Emanoel;
Correia Ferreira, Themístoclys Thesko;
de Souza Costa, Bruna Gabrielle;
Magalhães Soares, Rafaela;
Cruz de Lucena, Nahãmi;
de Barros Correia, Nancy

Publication type:

Article

Low-dose high-frequency enzyme replacement therapy for very young children with severe Gaucher...

Published in:

1994

By:

Zimran, A.;
Smith, Jeanette M.

Publication type:

Abstract

From the National Institutes of Health.

Published in:

1991

By:

Healy, Bernadine;
Healy, B

Publication type:

journal article

Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1.

Published in:

2018

By:

Zimmermann, Anca;
Popp, Radu A;
Rossmann, Heidi;
Bucerzan, Simona;
Nascu, Ioana;
Leucuta, Daniel;
Weber, Matthias M;
Grigorescu-Sido, Paula

Publication type:

journal article

Profile of eliglustat tartrate in the management of Gaucher disease.

Published in:

2016

By:

Sechi, Annalisa;
Dardis, Andrea;
Bembi, Bruno

Publication type:

journal article

Homozygosity for two mild glucocerebrosidase mutations of probable Iberian origin.

Published in:

Clinical Genetics, 1999, v. 56, n. 1, p. 100, doi. 10.1034/j.1399-0004.1999.560117.x

By:

Amaral, Olga;
Lacerda, Lucia;
Marcao, Ana;
Pinto, Eugenia;
Tamagnini, Gabriel;
Miranda, M.C. Sa

Publication type:

Article

Immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—The taliglucerase alfa story.

Published in:

PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0186211

By:

Rup, Bonita;
Alon, Sari;
Amit-Cohen, Bat-Chen;
Brill Almon, Einat;
Chertkoff, Raul;
Tekoah, Yoram;
Rudd, Pauline M.

Publication type:

Article

Reply to vom dahl et al.

Published in:

British Journal of Haematology, 2001, v. 113, n. 4, p. 1086, doi. 10.1046/j.1365-2141.2001.02821-10.x

By:

Elstein, Deborah;
Abrahamov, Aya;
Hadas-Halpern, Irith;
Zimran, Ari

Publication type:

Article

Interruption in enzyme replacement therapy for gaucher disease.

Published in:

British Journal of Haematology, 2001, v. 113, n. 4, p. 1087, doi. 10.1046/j.1365-2141.2001.02821-11.x

By:

Weinreb, Neal J.

Publication type:

Article

Withdrawal of enzyme replacement therapy in Gaucher's disease.

Published in:

British Journal of Haematology, 2000, v. 110, n. 2, p. 488, doi. 10.1046/j.1365-2141.2000.02177.x

By:

Elstein, Deborah;
Abrahamov, Ayala;
Hadas-Halpern, Irith;
Zimran, Ari

Publication type:

Article

2012 The year in review.

Published in:

Chemistry & Industry, 2012, v. 76, n. 11, p. 32

By:

O'Driscoll, Cath

Publication type:

Article

Novel Therapies.

Published in:: Current Medical Literature: Lysosomal Storage Disease, 2014, v. 12, n. 1, p. 26
Publication type:: Article

Novel Therapies.

Published in:: Current Medical Literature: Lysosomal Storage Disease, 2013, v. 11, n. 4, p. 122
Publication type:: Article

Taliglucerase alfa leads to favorable bone marrow responses in patients with type I Gaucher disease.

Published in:

2013

By:

Mehta, Atul

Publication type:

Opinion

Velaglucerase alfa enzyme replacement therapy compared with imiglucerase in patients with Gaucher disease.

Published in:

2013

By:

Mehta, Atul

Publication type:

Opinion

Altered innate function of plasmacytoid dendritic cells restored by enzyme replacement therapy in Gaucher disease.

Published in:

2013

By:

Mehta, Atul

Publication type:

Opinion

Successful desensitization to imiglucerase of an adult patient diagnosed with type I Gaucher disease.

Published in:

2013

By:

Mehta, Atul

Publication type:

Opinion

Gauchers disease - a reappraisal of hematopoietic stem cell transplantation.

Published in:

2013

By:

Mehta, Atul

Publication type:

Opinion

Evaluation of miglustat as maintenance therapy after enzyme therapy on adults with stable type 1 Gaucher disease: a prospective, open-label non-inferiority study.

Published in:

Current Medical Literature: Lysosomal Storage Disease, 2013, v. 11, n. 2, p. 49

By:

Cox, T. M.;
Amato, D.;
Hollak, C. E.

Publication type:

Article

Miscellaneous.

Published in:: Current Medical Literature: Lysosomal Storage Disease, 2013, v. 11, n. 1, p. 31
Publication type:: Article

Novel Therapies.

Published in:: Current Medical Literature: Lysosomal Storage Disease, 2013, v. 11, n. 1, p. 27
Publication type:: Article

Clinical Manifestations.

Published in:: Current Medical Literature: Lysosomal Storage Disease, 2013, v. 11, n. 1, p. 20
Publication type:: Article

Genetics.

Published in:: Current Medical Literature: Lysosomal Storage Disease, 2013, v. 11, n. 1, p. 12
Publication type:: Article

Enzyme/Protein-Replacement Therapy.

Published in:: Current Medical Literature: Lysosomal Storage Disease, 2013, v. 11, n. 1, p. 9
Publication type:: Article

Clinical Manifestations.

Published in:: 2012
Publication type:: Abstract

Management of Type 3 Gaucher Disease.

Published in:

Current Medical Literature: Lysosomal Storage Disease, 2012, v. 10, n. 4, p. 93

By:

Abdelwahab, Magy

Publication type:

Article

Enzyme/Protein Replacement Therapy.

Published in:: Current Medical Literature: Lysosomal Storage Disease, 2012, v. 10, n. 2, p. 54
Publication type:: Article

[1] Significant and continuous improvement in bone mineral density among type 1 Gaucher disease patients treated with velaglucerase alfa: 69-month experience, including dose reduction./Early achievement and maintenance of the therapeutic goals using velaglucerase alfa in type 1 Gaucher disease.

Published in:: Current Medical Literature: Lysosomal Storage Disease, 2012, v. 10, n. 1, p. 28
Publication type:: Article

Target identification: Targeting neuronal loss in Gaucher's disease.

Published in:

Nature Reviews Drug Discovery, 2014, v. 13, n. 3, p. 178, doi. 10.1038/nrd4270

By:

Harrison, Charlotte

Publication type:

Article

Glucocerebrosidase level in the cerebrospinal fluid during enzyme replacement therapy – unsuccessful treatment of the neurological abnormality in type 2 Gaucher disease.

Published in:

European Journal of Pediatrics, 2003, v. 162, n. 7/8, p. 524, doi. 10.1007/s00431-001-0859-7

By:

Migita, Makoto;
Hamada, Hisamitsu;
Fujimura, Juri;
Watanabe, Atsushi;
Shimada, Takashi;
Fukunaga, Yoshitaka

Publication type:

Article

Improvement of neurological symptoms by enzyme replacement therapy for Gaucher disease type IIIb.

Published in:

2001

By:

Aoki, Minako;
Takahashi, Yukitoshi;
Miwa, Yuka;
Iida, Satoko;
Sukegawa, Kazuko;
Horai, Toshio;
Orii, Tadao;
Kondo, Naomi;
Aoki, M;
Takahashi, Y;
Miwa, Y;
Iida, S;
Sukegawa, K;
Horai, T;
Orii, T;
Kondo, N

Publication type:

Case Study

Cellular Uptake of Glucocerebrosidase in Gaucher Patients Receiving Enzyme Replacement Treatment.

Published in:

2016

By:

Gras-Colomer, Elena;
Martínez-Gómez, María;
Moya-Gil, Ana;
Fernandez-Zarzoso, Miguel;
Merino-Sanjuan, Matilde;
Climente-Martí, Mónica;
Martínez-Gómez, María Amparo;
Climente-Martí, Mónica

Publication type:

journal article

Gaucher's Disease: Diagnosis and Treatment.

Published in:: American Family Physician, 1994, v. 49, n. 5, p. 1231
Publication type:: Article