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Charmed hadrons from coalescence plus fragmentation in relativistic nucleus-nucleus collisions at RHIC and LHC

The European physical journal. C, Particles and fields, 2018-04, Vol.78 (4), p.1-13, Article 348

2018

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Cluster formation near midrapidity: How the production mechanisms can be identified experimentally

Physical review. C, 2024-04, Vol.109 (4), Article 044906

2024

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COVID-19 complications in a small-town hospital in South Africa

South African medical journal, 2021-11, Vol.111 (11), p.1046-1049

2021

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Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes

Molecular cytogenetics, 2021-03, Vol.14 (1), p.17-17, Article 17

2021

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Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental Delay

Cytogenetic and genome research, 2023-05, Vol.162 (7), p.365-371

2023

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Clinical ultrasonography in loggerhead sea turtles (Caretta caretta): imaging of pathological features

Veterinární medicína, 2016-01, Vol.61 (3), p.155-161

2016

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Exploring two novel cases of suspected ictal epileptic headache, a rare form of paediatric epilepsy

Acta Paediatrica, 2017-05, Vol.106 (5), p.786-790

2017

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Novel Self-Inactivating Vectors for Reconstitution of Wiskott-Aldrich Syndrome

Current gene therapy, 2015-01, Vol.15 (3), p.245-254

2015

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Pyruvate carboxylase deficiency type A and type C: Characterization of five novel pathogenic variants in PC and analysis of the genotype–phenotype correlation

Human mutation, 2019-06, Vol.40 (6), p.816-827

2019

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Parton-hadron-quantum-molecular dynamics: A novel microscopic n -body transport approach for heavy-ion collisions, dynamical cluster formation, and hypernuclei production

Physical review. C, 2020-04, Vol.101 (4), Article 044905

2020

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Dynamical mechanisms for deuteron production at mid-rapidity in relativistic heavy-ion collisions from energies available at the GSI Schwerionensynchrotron to those at the BNL Relativistic Heavy Ion Collider

Physical review. C, 2023-07, Vol.108 (1), Article 014902

2023

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Novel homozygous missense mutation in ALDH7A1 causes neonatal pyridoxine dependent epilepsy

Molecular and cellular probes, 2017-04, Vol.32, p.18-23

2017

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7q11.23 microduplication syndrome: neurophysiological and neuroradiological insights into a rare chromosomal disorder

Journal of intellectual disability research, 2018-05, Vol.62 (5), p.359-370

2018

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Novel Unbalanced Translocations Affecting the Long Arms of Chromosomes 10 and 22 Cause Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy

Cytogenetic and genome research, 2017, Vol.151 (4), p.171-178

2017

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Development of Novel Efficient SIN Vectors with Improved Safety Features for Wiskott–Aldrich Syndrome Stem Cell Based Gene Therapy

Molecular pharmaceutics, 2011-10, Vol.8 (5), p.1525-1537

2011

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Direct flow of heavy mesons as unique probe of the initial Electro-Magnetic fields in Ultra-Relativistic Heavy Ion collisions

Nuclear physics. A, 2019-02, Vol.982, p.189-191

2019

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Transport properties from Charm to Bottom: p suppression, anisotropic flow ν and their correlations to the bulk dynamics

Nuclear physics. A, 2019-02, Vol.982, p.655-658

2019

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De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndrome

Clinical dysmorphology, 2018-07, Vol.27 (3), p.97-100

2018

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Unbalanced translocation affecting the long arms of chromosomes 10 and 22 causes complex syndromes with very severe neuro-developmental delay, speech impairment, autistic behavior and epilepsy

European journal of paediatric neurology, 2017-06, Vol.21, p.e72-e72

2017

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Novel homozygous missense mutation in ALDH7A1 causes neonatal pyridoxine dependent epilepsy

European journal of paediatric neurology, 2017-06, Vol.21, p.e99-e99

2017

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Impact of Glasma on heavy quark RAA and ν2 in nucleus-nucleus collisions at LHC

Nuclear physics. A, 2021-01, Vol.1005, p.121913, Article 121913

2021

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WITHDRAWN: Assessment of hematopoietic and neurologic pathophysiology of HCLS1-associated protein X-1 deficiency in a Hax1-knockout mouse model

Experimental hematology, 2014-10

2014

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Transport properties from Charm to Bottom: pT suppression, anisotropic flow νn and their correlations to the bulk dynamics

Nuclear physics. A, 2019-02, Vol.982, p.655-658

2019

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CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes

Molecular cytogenetics, 2016-02, Vol.9 (10), p.10-10

2016

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Efficacy of oxfendazole and fenbendazole against tortoise (Testudo hermanni) oxyurids

Parasitology research (1987), 2007-04, Vol.100 (5), p.1069-1073

2007

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Charmed hadrons from coalescence plus fragmentation in relativistic nucleus-nucleus collisions at RHIC and LHC

Cluster formation near midrapidity: How the production mechanisms can be identified experimentally

COVID-19 complications in a small-town hospital in South Africa

Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes

Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental Delay

Clinical ultrasonography in loggerhead sea turtles (Caretta caretta): imaging of pathological features

Exploring two novel cases of suspected ictal epileptic headache, a rare form of paediatric epilepsy

Novel Self-Inactivating Vectors for Reconstitution of Wiskott-Aldrich Syndrome

Pyruvate carboxylase deficiency type A and type C: Characterization of five novel pathogenic variants in PC and analysis of the genotype–phenotype correlation

Parton-hadron-quantum-molecular dynamics: A novel microscopic n -body transport approach for heavy-ion collisions, dynamical cluster formation, and hypernuclei production

Dynamical mechanisms for deuteron production at mid-rapidity in relativistic heavy-ion collisions from energies available at the GSI Schwerionensynchrotron to those at the BNL Relativistic Heavy Ion Collider

Novel homozygous missense mutation in ALDH7A1 causes neonatal pyridoxine dependent epilepsy

7q11.23 microduplication syndrome: neurophysiological and neuroradiological insights into a rare chromosomal disorder

Novel Unbalanced Translocations Affecting the Long Arms of Chromosomes 10 and 22 Cause Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy

Development of Novel Efficient SIN Vectors with Improved Safety Features for Wiskott–Aldrich Syndrome Stem Cell Based Gene Therapy

Direct flow of heavy mesons as unique probe of the initial Electro-Magnetic fields in Ultra-Relativistic Heavy Ion collisions

Transport properties from Charm to Bottom: p suppression, anisotropic flow ν and their correlations to the bulk dynamics

De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndrome

Unbalanced translocation affecting the long arms of chromosomes 10 and 22 causes complex syndromes with very severe neuro-developmental delay, speech impairment, autistic behavior and epilepsy

Novel homozygous missense mutation in ALDH7A1 causes neonatal pyridoxine dependent epilepsy

Impact of Glasma on heavy quark RAA and ν2 in nucleus-nucleus collisions at LHC

WITHDRAWN: Assessment of hematopoietic and neurologic pathophysiology of HCLS1-associated protein X-1 deficiency in a Hax1-knockout mouse model

Transport properties from Charm to Bottom: pT suppression, anisotropic flow νn and their correlations to the bulk dynamics

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes

Efficacy of oxfendazole and fenbendazole against tortoise (Testudo hermanni) oxyurids

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