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Cultural Adaptation of the Portuguese Version of the "Sniffin' Sticks" Smell Test: Reliability, Validity, and Normative Data

PloS one, 2016-02, Vol.11 (2), p.e0148937-e0148937

2016

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Novel Insights in the Management of Vernal Keratoconjunctivitis (VKC): European Expert Consensus Using a Modified Nominal Group Technique

Ophthalmology and therapy, 2023-04, Vol.12 (2), p.1207-1222

2023

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ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous

Human molecular genetics, 2012-08, Vol.21 (16), p.3681-3694

2012

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Amblyopia screening effectiveness at 3–4 years old: a cohort study

BMJ open ophthalmology, 2021-01, Vol.6 (1), p.e000599-e000599

2021

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Extreme Hyperopia Is the Result of Null Mutations in MFRP, Which Encodes a Frizzled-Related Protein

Proceedings of the National Academy of Sciences - PNAS, 2005-07, Vol.102 (27), p.9553-9558

2005

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Distribution Systems Planning Considering Operational Performance and Power Quality Indices

Journal of control, automation & electrical systems, 2021-12, Vol.32 (6), p.1678-1689

2021

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Distribution of potential suitable hammers and transport of hammer tools and nuts by wild capuchin monkeys

Primates, 2009-04, Vol.50 (2), p.95-104

2009

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Genetic basis of total colourblindness among the Pingelapese islanders

Nature genetics, 2000-07, Vol.25 (3), p.289-293

2000

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The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in thePISD gene

Genetics in medicine, 2019-12, Vol.21 (12), p.2734-2743

2019

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Brain damage serum biomarkers induced by COVID-19 in patients from northeast Brazil

Journal of neurovirology, 2023-04, Vol.29 (2), p.180-186

2023

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Horizontal Gaze Palsy and Progressive Scoliosis in Dizygotic Twins

Journal of binocular vision and ocular motility, 2022-04, Vol.72 (2), p.105-110

2022

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Continuing professional development: best practices

Middle East African journal of ophthalmology, 2014-04, Vol.21 (2), p.134-141

2014

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Optic pit: novel surgical management of complicated cases

Retina (Philadelphia, Pa.), 2013-09, Vol.33 (8), p.1708-1714

2013

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Neural correlates of visual integration in Williams syndrome: Gamma oscillation patterns in a model of impaired coherence

Neuropsychologia, 2013-06, Vol.51 (7), p.1287-1295

2013

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Cross-cultural validation of a taste test with paper strips

European archives of oto-rhino-laryngology, 2016-10, Vol.273 (10), p.3407-3411

2016

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Accelerated age-related olfactory decline among type 1 Usher patients

Scientific reports, 2016-06, Vol.6 (1), p.28309-28309, Article 28309

2016

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The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in the PISD gene

Genetics in medicine, 2019-12, Vol.21 (12), p.2734-2743

2019

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Novel de novo FOXC1 nonsense mutation in an Axenfeld‐Rieger syndrome patient

American journal of medical genetics. Part A, 2017-06, Vol.173 (6), p.1607-1610

2017

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Gyrification, cortical and subcortical morphometry in neurofibromatosis type 1: an uneven profile of developmental abnormalities

Journal of neurodevelopmental disorders, 2013-02, Vol.5 (1), p.3-3, Article 3

2013

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Evidence of Widespread Retinal Dysfunction in Patients with Stargardt Disease and Morphologically Unaffected Carrier Relatives

Investigative ophthalmology & visual science, 2008-03, Vol.49 (3), p.1191-1199

2008

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Abnormal late visual responses and alpha oscillations in neurofibromatosis type 1: a link to visual and attention deficits

Journal of neurodevelopmental disorders, 2014-02, Vol.6 (1), p.4-4, Article 4

2014

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Influence of taurine on the zootechnical performance and health parameters of juvenile Nile tilapia in a recirculating aquaculture system

Anais da Academia Brasileira de Ciências, 2024-01, Vol.96 (2), p.e20230892-e20230892

2024

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Development and evaluation of an inhalation chamber for in vivo tests

Anais da Academia Brasileira de Ciências, 2017-07, Vol.89 (3), p.1643-1653

2017

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Cryptic 7q36.2q36.3 deletion causes multiple congenital eye anomalies and craniofacial dysmorphism

American journal of medical genetics. Part A, 2013-03, Vol.161 (3), p.589-593

2013

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Evaluation of compressive strength in geopolymer mortars produced using iron ore tailings ground by tumbling ball mills

Tecnologia em metalurgia, materiais e mineração, 2021, Vol.18, p.e2480

2021

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Cultural Adaptation of the Portuguese Version of the "Sniffin' Sticks" Smell Test: Reliability, Validity, and Normative Data

Novel Insights in the Management of Vernal Keratoconjunctivitis (VKC): European Expert Consensus Using a Modified Nominal Group Technique

ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous

Amblyopia screening effectiveness at 3–4 years old: a cohort study

Extreme Hyperopia Is the Result of Null Mutations in MFRP, Which Encodes a Frizzled-Related Protein

Distribution Systems Planning Considering Operational Performance and Power Quality Indices

Distribution of potential suitable hammers and transport of hammer tools and nuts by wild capuchin monkeys

Genetic basis of total colourblindness among the Pingelapese islanders

The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in thePISD gene

Brain damage serum biomarkers induced by COVID-19 in patients from northeast Brazil

Horizontal Gaze Palsy and Progressive Scoliosis in Dizygotic Twins

Continuing professional development: best practices

Optic pit: novel surgical management of complicated cases

Neural correlates of visual integration in Williams syndrome: Gamma oscillation patterns in a model of impaired coherence

Cross-cultural validation of a taste test with paper strips

Accelerated age-related olfactory decline among type 1 Usher patients

The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in the PISD gene

Novel de novo FOXC1 nonsense mutation in an Axenfeld‐Rieger syndrome patient

Gyrification, cortical and subcortical morphometry in neurofibromatosis type 1: an uneven profile of developmental abnormalities

Evidence of Widespread Retinal Dysfunction in Patients with Stargardt Disease and Morphologically Unaffected Carrier Relatives

Abnormal late visual responses and alpha oscillations in neurofibromatosis type 1: a link to visual and attention deficits

Influence of taurine on the zootechnical performance and health parameters of juvenile Nile tilapia in a recirculating aquaculture system

Development and evaluation of an inhalation chamber for in vivo tests

Cryptic 7q36.2q36.3 deletion causes multiple congenital eye anomalies and craniofacial dysmorphism

Evaluation of compressive strength in geopolymer mortars produced using iron ore tailings ground by tumbling ball mills

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