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Refinado por: tipo de recurso: Reports remover
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1
Varicella with palmoplantar involvement: Presentation of a case
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Report
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Varicella with palmoplantar involvement: Presentation of a case

Huesa Andrade, M ; González Lavandeira, M

Semergen, 2016, Vol.42 (8), p.593-595

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2
The Importance of Patient Empowerment: A Clinical Case of Hereditary Angioedem
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The Importance of Patient Empowerment: A Clinical Case of Hereditary Angioedem

Santos, Guida Maria ; Andrade, Filipa M ; Marrana, Catarina ; Gouveia, Sara

Cureus, 2023, Vol.15 (10), p.e47644-e47644

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3
Primary Deforming and Reversible Arthropathy: A Variant of Jaccoud Arthropathy?
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Report
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Primary Deforming and Reversible Arthropathy: A Variant of Jaccoud Arthropathy?

Santiago, Mittermayer B ; de Sousa Braz, Alessandra ; Freire, Eutilia Andrade M ; de Lucena, Germana Ribeiro A C ; Almeida, Bruna Laiza F ; Ribeiro, Daniel Sá

Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases, 2015, Vol.21 (8), p.455-456

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4
Beyond Borders: Monkeypox Case on Madeira Island
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Beyond Borders: Monkeypox Case on Madeira Island

Andrade, Filipa M ; Faria, Guilherme N ; Ramos, Maria L ; Franco, Susana ; Sardinha, Tiago ; Gouveia, Sara

Cureus, 2023, Vol.15 (12), p.e50715-e50715

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5
Balanced chromosomal rearrangement in a partner revealed after Preimplantation Genetic Testing for Aneuploidies (PGT-A)
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Balanced chromosomal rearrangement in a partner revealed after Preimplantation Genetic Testing for Aneuploidies (PGT-A)

Ceschin, Ianaê ; Ali, Taccyanna M ; Carvalho, Cristina V ; Martins, Caique ; Bos-Mikich, Adriana ; Andrade, Gabriella M ; Frantz, Nilo

JBRA assisted reproduction, 2023, Vol.27 (2), p.320-324

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6
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)
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Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)

Thompson, Miles D ; Li, Xueying ; Spencer-Manzon, Michele ; Andrade, Danielle M ; Murakami, Yoshiko ; Kinoshita, Taroh ; Carpenter, Thomas O

Genes, 2023, Vol.14 (2)

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7
New liposomal cytarabine formulation in CSF
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New liposomal cytarabine formulation in CSF

Casado, P ; Torreira, C ; Oujo, E ; Esteban, P ; Albo, C ; Diaz, R ; Andrade, M A

Clinical laboratory, 2010, Vol.56 (1-2), p.69-70

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8
Seizures and early onset dementia: D2HGA1 inborn error of metabolism in adults
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Seizures and early onset dementia: D2HGA1 inborn error of metabolism in adults

Tabarestani, Sepideh ; Varriano, Brenda ; Rawal, Sapna ; France Morel, Chantal ; Carmela Tartaglia, Maria ; Andrade, Danielle M

Annals of clinical and translational neurology, 2020, Vol.7 (10), p.2052-2056

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9
Cerebral Corticoarterial Malformations : A Case Series of Unilateral Polymicrogyria and Ipsilateral Arterial Dysplasia
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Report
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Cerebral Corticoarterial Malformations : A Case Series of Unilateral Polymicrogyria and Ipsilateral Arterial Dysplasia

Klostranec, Jesse M ; Brinjikji, Waleed ; Mathur, Shobhit ; Orru, Emanuele ; Andrade, Danielle M ; Krings, Timo

Clinical neuroradiology, 2020, Vol.30 (2), p.389-394

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10
Massive intrasplenic arterial thrombosis in a patient with chronic ITP during the development of an Evans syndrome
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Report
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Massive intrasplenic arterial thrombosis in a patient with chronic ITP during the development of an Evans syndrome

Diez-Feijóo, R ; Rodríguez-Sevilla, J J ; Colomo, L ; Papaleo, N ; Maiques, J M ; Gimeno, E ; Andrade-Campos, M ; Abella, E ; Merchan, B M ; Calvo, X ; Jimenez, C ; Román-Bravo, O D ; Salar, A ; Sanchez-Gonzalez, B

Thrombosis research, 2021, Vol.208, p.226-229

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