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Vitamin D in health and disease: a literature review

British journal of biomedical science, 2013-01, Vol.70 (4), p.161-172

Basit, S.

2013

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Comparison of second cancer risk due to out-of-field doses from 6-MV IMRT and proton therapy based on 6 pediatric patient treatment plans

Radiotherapy and oncology, 2011-01, Vol.98 (1), p.87-92

2011

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Assessment of radiation-induced second cancer risks in proton therapy and IMRT for organs inside the primary radiation field

Physics in medicine & biology, 2012-10, Vol.57 (19), p.6047-6061

2012

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Genetics of human isolated hereditary hair loss disorders

Clinical genetics, 2015-09, Vol.88 (3), p.203-212

2015

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Neutron equivalent doses and associated lifetime cancer incidence risks for head & neck and spinal proton therapy

Physics in medicine & biology, 2009-08, Vol.54 (16), p.4907-4926

2009

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First direct evidence of involvement of a homozygous loss‐of‐function variant in the EPS15L1 gene underlying split‐hand/split‐foot malformation

Clinical genetics, 2018-03, Vol.93 (3), p.699-702

2018

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Developmental dysplasia of the hip: usefulness of next generation genomic tools for characterizing the underlying genes - a mini review

Clinical genetics, 2016-07, Vol.90 (1), p.16-20

2016

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Comparison of out-of-field photon doses in 6 MV IMRT and neutron doses in proton therapy for adult and pediatric patients

Physics in medicine & biology, 2010-05, Vol.55 (10), p.2879-2891

2010

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Whole exome sequencing enables the correct diagnosis of Frank–Ter Haar syndrome in a Saudi family

Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii, 2024-06, Vol.28 (3), p.326-331

2024

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Woodhouse–Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene

Clinical and experimental dermatology, 2020-03, Vol.45 (2), p.159-164

2020

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VP37.02: Reference ranges for maternal cardiovascular profiles in normal pregnancies

Ultrasound in obstetrics & gynecology, 2021-10, Vol.58 (S1), p.253-253

2021

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VP34.03: Is there an association between the size of the decline in maternal cardiac output in the third trimester and offspring birthweight?

Ultrasound in obstetrics & gynecology, 2021-10, Vol.58 (S1), p.89-312

2021

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Genetics of human isolated hereditary nail disorders

British journal of dermatology (1951), 2015-10, Vol.173 (4), p.922-929

2015

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The Paediatric Cataract Register (PECARE): an overview of operated childhood cataract in Sweden and Denmark

Acta ophthalmologica (Oxford, England), 2018-02, Vol.96 (1), p.51-55

2018

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Effect of particle size distribution on magnetic behavior of nanoparticles with uniaxial anisotropy

Chinese physics B, 2018-09, Vol.27 (9), p.97503

2018

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A homozygous potentially pathogenic variant in the PAXBP1 gene in a large family with global developmental delay and myopathic hypotonia

Clinical genetics, 2017-12, Vol.92 (6), p.579-586

2017

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PB1896: WHOLE EXOME SEQUENCING IDENTIFIES A NOVEL TRANSCRIPTION FACTOR ASSOCIATED WITH FATAL DISEASE PROGRESSION IN CHRONIC MYELOID LEUKEMIA

HemaSphere, 2022-06, Vol.6 (Suppl), p.1775-1776

2022

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Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia

Clinical genetics, 2017-03, Vol.91 (3), p.494-498

2017

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Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families

Clinical and experimental dermatology, 2018-08, Vol.43 (6), p.752-755

2018

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A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation

Clinical genetics, 2012-07, Vol.82 (1), p.48-55

2012

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Adjuvant radiation therapy for early stage seminoma: Proton versus photon planning comparison and modeling of second cancer risk

Radiotherapy and oncology, 2012-04, Vol.103 (1), p.12-17

2012

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Exploiting Machine Learning to Detect Malicious Nodes in Intelligent Sensor-Based Systems Using Blockchain

Wireless communications and mobile computing, 2022-01, Vol.2022, p.1-16

2022

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New Trends and Advancement in Next Generation Mobile Wireless Communication (6G): A Survey

Wireless communications and mobile computing, 2021-12, Vol.2021, p.1-14

2021

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Dose-Rate Effects When Estimating Risks for Second Malignancies: In Regard to Fontenot et al ( Int J Radiat Oncol Biol Phys 2009;74:616–622)

International journal of radiation oncology, biology, physics, 2009-12, Vol.75 (5), p.1624-1624

2009

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Reducing the Sidelobes in Doppler-Range Beam Pattern and Controlling the Frequency Channel in SIAR

Wireless communications and mobile computing, 2023-08, Vol.2023, p.1-12

2023

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Vitamin D in health and disease: a literature review

Comparison of second cancer risk due to out-of-field doses from 6-MV IMRT and proton therapy based on 6 pediatric patient treatment plans

Assessment of radiation-induced second cancer risks in proton therapy and IMRT for organs inside the primary radiation field

Genetics of human isolated hereditary hair loss disorders

Neutron equivalent doses and associated lifetime cancer incidence risks for head & neck and spinal proton therapy

First direct evidence of involvement of a homozygous loss‐of‐function variant in the EPS15L1 gene underlying split‐hand/split‐foot malformation

Developmental dysplasia of the hip: usefulness of next generation genomic tools for characterizing the underlying genes - a mini review

Comparison of out-of-field photon doses in 6 MV IMRT and neutron doses in proton therapy for adult and pediatric patients

Whole exome sequencing enables the correct diagnosis of Frank–Ter Haar syndrome in a Saudi family

Woodhouse–Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene

VP37.02: Reference ranges for maternal cardiovascular profiles in normal pregnancies

VP34.03: Is there an association between the size of the decline in maternal cardiac output in the third trimester and offspring birthweight?

Genetics of human isolated hereditary nail disorders

The Paediatric Cataract Register (PECARE): an overview of operated childhood cataract in Sweden and Denmark

Effect of particle size distribution on magnetic behavior of nanoparticles with uniaxial anisotropy

A homozygous potentially pathogenic variant in the PAXBP1 gene in a large family with global developmental delay and myopathic hypotonia

PB1896: WHOLE EXOME SEQUENCING IDENTIFIES A NOVEL TRANSCRIPTION FACTOR ASSOCIATED WITH FATAL DISEASE PROGRESSION IN CHRONIC MYELOID LEUKEMIA

Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia

Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families

A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation

Adjuvant radiation therapy for early stage seminoma: Proton versus photon planning comparison and modeling of second cancer risk

Exploiting Machine Learning to Detect Malicious Nodes in Intelligent Sensor-Based Systems Using Blockchain

New Trends and Advancement in Next Generation Mobile Wireless Communication (6G): A Survey

Dose-Rate Effects When Estimating Risks for Second Malignancies: In Regard to Fontenot et al ( Int J Radiat Oncol Biol Phys 2009;74:616–622)

Reducing the Sidelobes in Doppler-Range Beam Pattern and Controlling the Frequency Channel in SIAR

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