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Reversal of Intestinal Failure With Teduglutide in PERCC1 -Associated Enteropathy: A Case Report.
- Published in:
- Annals of Internal Medicine, 2024, v. 177, n. 8, p. 1141, doi. 10.7326/M24-0147
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- Publication type:
- Article
Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy.
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- Human Genetics, 2023, v. 142, n. 5, p. 691, doi. 10.1007/s00439-022-02486-1
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- Article
Hereditary orotic aciduria identified by newborn screening.
- Published in:
- Frontiers in Genetics, 2023, v. 14, p. 1, doi. 10.3389/fgene.2023.1135267
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- Article
Addition of galactose‐1‐phosphate measurement enhances newborn screening for classical galactosemia.
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- Journal of Inherited Metabolic Disease, 2023, v. 46, n. 2, p. 232, doi. 10.1002/jimd.12580
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- Article
Oculocutaneous albinism and bleeding diathesis due to a novel deletion in the HPS3 gene.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.936064
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- Article
Progressive pulmonary fibrosis in a murine model of Hermansky-Pudlak syndrome.
- Published in:
- 2022
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- Publication type:
- journal article
What Can We Learn from the Parents of Children Affected with Mucopolysaccharidosis Type III-A in Israel?
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- Molecular Syndromology, 2022, v. 13, n. 1, p. 45, doi. 10.1159/000519099
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- Publication type:
- Article
Deep intronic variant in the ARSB gene as the genetic cause for Maroteaux–Lamy syndrome (MPS VI).
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- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 12, p. 3804, doi. 10.1002/ajmg.a.62453
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- Article
The Effects of a Ketogenic Diet on Patients with Dihydrolipoamide Dehydrogenase Deficiency.
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- Nutrients, 2021, v. 13, n. 10, p. 3523, doi. 10.3390/nu13103523
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- Publication type:
- Article
The effects of the COVID-19 pandemic on patients with lysosomal storage disorders in Israel.
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- 2021
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- Publication type:
- journal article
Dietary-Induced Ketogenesis: Adults Are Not Children.
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- Nutrients, 2021, v. 13, n. 9, p. 3093, doi. 10.3390/nu13093093
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- Publication type:
- Article
A Phase I clinical trial of dose-escalated metabolic therapy combined with concomitant radiation therapy in high-grade glioma.
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- Journal of Neuro-Oncology, 2021, v. 153, n. 3, p. 487, doi. 10.1007/s11060-021-03786-8
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- Article
The role of orotic acid measurement in routine newborn screening for urea cycle disorders.
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- Journal of Inherited Metabolic Disease, 2021, v. 44, n. 3, p. 606, doi. 10.1002/jimd.12331
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- Publication type:
- Article
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.
- Published in:
- 2020
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- Publication type:
- Correction Notice
A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 5, p. 987, doi. 10.1002/ajmg.a.61509
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- Publication type:
- Article
Long-Term Outcomes of Early Enzyme Replacement Therapy for Mucopolysaccharidosis IV: Clinical Case Studies of Two Siblings.
- Published in:
- Diagnostics (2075-4418), 2020, v. 10, n. 2, p. 108, doi. 10.3390/diagnostics10020108
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- Publication type:
- Article
Netrin‐G2 dysfunction causes a Rett‐like phenotype with areflexia.
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- Human Mutation, 2020, v. 41, n. 2, p. 476, doi. 10.1002/humu.23945
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- Publication type:
- Article
Novel homozygous ENPP1 mutation causes generalized arterial calcifications of infancy, thrombocytopenia, and cardiovascular and central nervous system syndrome.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 10, p. 2112, doi. 10.1002/ajmg.a.61334
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- Publication type:
- Article
Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children.
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- Pediatric Nephrology, 2019, v. 34, n. 9, p. 1607, doi. 10.1007/s00467-019-04256-0
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- Publication type:
- Article
Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies.
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- Pediatric Rheumatology, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s12969-019-0349-y
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- Publication type:
- Article
Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature.
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- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0787-x
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- Publication type:
- Article
Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric Syndrome.
- Published in:
- 2018
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- Publication type:
- journal article
Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 12, p. 2273, doi. 10.1007/s00467-017-3755-8
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- Publication type:
- Article
Clinically Distinct Phenotypes of Canavan Disease Correlate with Residual Aspartoacylase Enzyme Activity.
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- Human Mutation, 2017, v. 38, n. 5, p. 524, doi. 10.1002/humu.23181
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- Publication type:
- Article
A Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF).
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- Journal of Clinical Immunology, 2016, v. 36, n. 8, p. 801, doi. 10.1007/s10875-016-0340-z
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- Publication type:
- Article
Expanding the molecular diversity and phenotypic spectrum of glycerol 3-phosphate dehydrogenase 1 deficiency.
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- Journal of Inherited Metabolic Disease, 2016, v. 39, n. 5, p. 689, doi. 10.1007/s10545-016-9956-7
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- Publication type:
- Article
Primary and maternal 3-methylcrotonyl-CoA carboxylase deficiency: insights from the Israel newborn screening program.
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- Journal of Inherited Metabolic Disease, 2016, v. 39, n. 2, p. 211, doi. 10.1007/s10545-015-9899-4
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- Publication type:
- Article
CAOS—Episodic Cerebellar Ataxia, Areflexia, Optic Atrophy, and Sensorineural Hearing Loss.
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- Journal of Child Neurology, 2015, v. 30, n. 13, p. 1749, doi. 10.1177/0883073815579708
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- Publication type:
- Article
Griscelli Syndrome Type 3: Two New Cases and Review of the Literature.
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- Pediatric Dermatology, 2015, v. 32, n. 6, p. e245, doi. 10.1111/pde.12663
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- Publication type:
- Article
Costeff syndrome: clinical features and natural history.
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- Journal of Neurology, 2014, v. 261, n. 12, p. 2275, doi. 10.1007/s00415-014-7481-x
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- Publication type:
- Article
Phenylbutyrate increases pyruvate dehydrogenase complex activity in cells harboring a variety of defects.
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- Annals of Clinical & Translational Neurology, 2014, v. 1, n. 7, p. 462, doi. 10.1002/acn3.73
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- Publication type:
- Article
Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood.
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- Brain: A Journal of Neurology, 2014, v. 137, n. 4, p. 1107, doi. 10.1093/brain/awu022
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- Article
The Many Faces of Glut1 Deficiency Syndrome.
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- Journal of Child Neurology, 2014, v. 29, n. 3, p. 349, doi. 10.1177/0883073812471718
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- Publication type:
- Article
A Human Integrin-α3 Mutation Confers Major Renal Developmental Defects.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0090879
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- Article
Neonatal Hyperpigmentation: Diagnosis of Familial Glucocorticoid Deficiency with a Novel Mutation in the Melanocortin-2 Receptor Gene.
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- Pediatric Dermatology, 2014, v. 31, n. 1, p. e13, doi. 10.1111/pde.12247
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- Publication type:
- Article
Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature.
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- Journal of Inherited Metabolic Disease, 2013, v. 36, n. 6, p. 923, doi. 10.1007/s10545-012-9580-0
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- Publication type:
- Article
Murine isoforms of UDP-GlcNAc 2-epimerase/ManNAc kinase: Secondary structures, expression profiles, and response to ManNAc therapy.
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- Glycoconjugate Journal, 2013, v. 30, n. 6, p. 609, doi. 10.1007/s10719-012-9459-1
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- Publication type:
- Article
Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia.
- Published in:
- Human Genetics, 2012, v. 131, n. 11, p. 1805, doi. 10.1007/s00439-012-1207-x
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- Publication type:
- Article
Estimating the Allele Frequency of Autosomal Recessive Disorders through Mutational Records and Consanguinity: The Homozygosity Index (HI).
- Published in:
- Annals of Human Genetics, 2012, v. 76, n. 2, p. 159, doi. 10.1111/j.1469-1809.2011.00693.x
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- Publication type:
- Article
Cellular and clinical report of new Griscelli syndrome type III cases.
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- Pigment Cell & Melanoma Research, 2012, v. 25, n. 1, p. 47, doi. 10.1111/j.1755-148X.2011.00901.x
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- Publication type:
- Article
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet ?-granules.
- Published in:
- Nature Genetics, 2011, v. 43, n. 8, p. 732, doi. 10.1038/ng.883
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- Publication type:
- Article
Ex Vivo Treatment with a Novel Synthetic Aminoglycoside NB54 in Primary Fibroblasts from Rett Syndrome Patients Suppresses MECP2 Nonsense Mutations.
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- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0020733
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- Publication type:
- Article
Metabolic acetate therapy improves phenotype in the tremor rat model of Canavan disease.
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- Journal of Inherited Metabolic Disease, 2010, v. 33, n. 3, p. 195, doi. 10.1007/s10545-010-9100-z
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- Publication type:
- Article
DHPLC screening for mutations in progressive familial intrahepatic cholestasis patients.
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- Journal of Human Genetics, 2010, v. 55, n. 5, p. 308, doi. 10.1038/jhg.2010.28
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- Publication type:
- Article
Clinical and genetic heterogeneity of congenital adrenal hypoplasia due to NR0B1 gene mutations.
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- Clinical Endocrinology, 2010, v. 72, n. 4, p. 448, doi. 10.1111/j.1365-2265.2009.03652.x
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- Article
Carbonic Anhydrase II Deficiency: A Novel Mutation.
- Published in:
- 2009
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- Publication type:
- Case Study
Genotype–phenotype correlations analysis of mutations in the phenylalanine hydroxylase ( PAH) gene.
- Published in:
- Journal of Human Genetics, 2008, v. 53, n. 5, p. 407, doi. 10.1007/s10038-008-0264-4
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- Publication type:
- Article
Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy in Isolated Sulfite Oxidase Deficiency.
- Published in:
- Journal of Child Neurology, 2007, v. 22, n. 10, p. 1214, doi. 10.1177/0883073807306260
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- Publication type:
- Article
A new genetic isolate with a unique phenotype of syndromic oculocutaneous albinism: clinical, molecular, and cellular characteristics.
- Published in:
- Human Mutation, 2006, v. 27, n. 11, p. 1158, doi. 10.1002/humu.9463
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- Publication type:
- Article
Unusual Presentation of Familial Glucocorticoid Deficiency with a Novel MRAP Mutation.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 10, p. 3713, doi. 10.1210/jc.2006-0687
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- Publication type:
- Article