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Almeida-Quintana, Lourdes
230  Ergebnisse:
Personensuche X
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1

A catalog of the genetic causes of hereditary angioedema in..:

Mendoza-Alvarez, Alejandro ; Tosco-Herrera, Eva ; Muñoz-Barrera, Adrian...
Frontiers in Immunology.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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2

First Census of Patients with Hereditary Angioedema in the ..:

Mendoza-Alvarez, Alejandro ; Marcelino-Rodriguez, Itahisa ; Almeida-Quintana, Lourdes...
Journal of Clinical Medicine.  10 (2021)  20 - p. 4711 , 2021
Link: https://doi.org/10.3390/..
 
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3

A catalog of the genetic causes of hereditary angioedema in..:

Mendoza-Alvarez, Alejandro ; Tosco-Herrera, Eva ; Muñoz-Barrera, Adrian...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531158/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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4

First Census of Patients with Hereditary Angioedema in the ..:

Mendoza-Alvarez, Alejandro ; Marcelino-Rodriguez, Itahisa ; Almeida-Quintana, Lourdes...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540601/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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5

Table_1_A catalog of the genetic causes of hereditary angio..:

Alejandro Mendoza-Alvarez ; Eva Tosco-Herrera ; Adrian Muñoz-Barrera...
doi:10.3389/fimmu.2022.997148.s001.  , 2022
Link: https://doi.org/10.3389/..
 
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6

A catalog of the genetic causes of hereditary angioedema in..:

Alejandro Mendoza-Alvarez ; Eva Tosco-Herrera ; Adrian Muñoz-Barrera...
https://www.frontiersin.org/articles/10.3389/fimmu.2022.997148/full.  , 2022
Link: https://doi.org/10.3389/..
 
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7

First Census of Patients with Hereditary Angioedema in the ..:

Alejandro Mendoza-Alvarez ; Itahisa Marcelino-Rodriguez ; Lourdes Almeida-Quintana...
https://www.mdpi.com/2077-0383/10/20/4711.  , 2021
Link: https://doi.org/10.3390/..
 
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8

First Census of Patients with Hereditary Angioedema in the ..:

Alejandro Mendoza-Alvarez ; Itahisa Marcelino-Rodriguez ; Lourdes Almeida-Quintana...
Vascular Medicine.  , 2021
Link: https://doi.org/10.3390/..
 
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9

Improving the diagnosis of cobalamin and related defects by..:

Brasil, Sandra ; Leal, Fátima ; Vega, Ana...
Orphanet Journal of Rare Diseases.  13 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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10

Improving the diagnosis of cobalamin and related defects by..:

Brasil, Sandra ; Leal, Fátima ; Vega, Ana...
Orphanet Journal of Rare Diseases.  , 2019
Link: http://hdl.handle.net/10..
 
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11

Improving the diagnosis of cobalamin and related defects by..:

Brasil, Sandra ; Leal, Fátima ; Vega, Ana...
http://hdl.handle.net/10668/12749.  , 2018
Link: http://hdl.handle.net/10..
 
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12

Improving the diagnosis of cobalamin and related defects by..:

Brasil, Sandra ; Leal, Fátima ; Vega, Ana...
Publisher's version.  , 2018
Link: http://hdl.handle.net/10..
 
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13

Improving the diagnosis of cobalamin and related defects by..:

Brasil, Sandra ; Leal, Fátima ; Vega, Ana...
http://hdl.handle.net/10668/12749.  , 2018
Link: http://hdl.handle.net/10..
 
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14

Improving the diagnosis of cobalamin and related defects by..:

Brasil, Sandra ; Leal, Fátima ; Vega, Ana...
Instituto de Salud Carlos III PI13-01239.  , 2018
Link: https://ddd.uab.cat/reco..
 
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15

Improving the diagnosis of cobalamin and related defects by..:

Brasil, Sandra ; Leal, Fátima ; Vega, Ana...
http://hdl.handle.net/10668/12749.  , 2018
Link: http://hdl.handle.net/10..
 
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