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  1. Article ; Online: A

    Fernandes, Priyanka / Howland, Shanshan W / Heiss, Kirsten / Hoffmann, Angelika / Hernández-Castañeda, Maria A / Obrová, Klára / Frank, Roland / Wiedemann, Philipp / Bendzus, Martin / Rénia, Laurent / Mueller, Ann-Kristin

    Frontiers in immunology

    2018  Volume 9, Page(s) 1875

    Abstract: Cerebral malaria is a complex neurological syndrome caused by an infection ... ...

    Abstract Cerebral malaria is a complex neurological syndrome caused by an infection with
    MeSH term(s) Animals ; Antigens, Protozoan/immunology ; CD8-Positive T-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/metabolism ; Cross-Priming/immunology ; Disease Models, Animal ; Disease Susceptibility ; Gene Expression ; Genes, Protozoan ; Genes, Reporter ; Life Cycle Stages ; Magnetic Resonance Imaging ; Malaria, Cerebral/diagnosis ; Malaria, Cerebral/immunology ; Malaria, Cerebral/parasitology ; Malaria, Cerebral/pathology ; Mice ; Plasmodium berghei/genetics ; Plasmodium berghei/growth & development ; Plasmodium berghei/immunology
    Chemical Substances Antigens, Protozoan
    Language English
    Publishing date 2018-08-14
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2018.01875
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  2. Article ; Online: European survey on the management of scabies by dermatologists in children under 2 months, pregnancy and breastfeeding woman.

    Sánchez-Díaz, Manuel / Hernández-Martín, Ángela / Descalzo, Miguel Ángel / García-Doval, Ignacio / Salavastru, Carmen Maria

    Journal of the European Academy of Dermatology and Venereology : JEADV

    2024  

    Language English
    Publishing date 2024-04-02
    Publishing country England
    Document type Letter
    ZDB-ID 1128828-0
    ISSN 1468-3083 ; 0926-9959
    ISSN (online) 1468-3083
    ISSN 0926-9959
    DOI 10.1111/jdv.20005
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    In stock of ZB MED Cologne/Königswinter

    Zs.A 3492: Show issues Location:
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  3. Article ; Online: A congenital folliculosebaceous cystic hamartoma on the nipple and areola.

    Blicharz, Leszek / Colmenero, Isabel / Hernández-Martín, Angela / Torrelo, Antonio

    International journal of dermatology

    2023  Volume 62, Issue 8, Page(s) e458–e460

    MeSH term(s) Humans ; Nipples ; Skin Neoplasms ; Follicular Cyst ; Neoplasms, Basal Cell ; Hamartoma/diagnosis
    Language English
    Publishing date 2023-04-23
    Publishing country England
    Document type Letter
    ZDB-ID 412254-9
    ISSN 1365-4632 ; 0011-9059 ; 1461-1244
    ISSN (online) 1365-4632
    ISSN 0011-9059 ; 1461-1244
    DOI 10.1111/ijd.16701
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  4. Article ; Online: T-wave inversion in young athletes: Normal or pathological?

    Aldomà-Balasch, Albina / Hernández-Martín, Ma Isabel / Viles-Bertran, Ma Dolors

    Archivos de cardiologia de Mexico

    2023  Volume 93, Issue 1, Page(s) 96–97

    MeSH term(s) Humans ; Arrhythmias, Cardiac ; Athletes ; Electrocardiography
    Language English
    Publishing date 2023-02-02
    Publishing country Mexico
    Document type Journal Article
    ZDB-ID 2059019-2
    ISSN 1665-1731 ; 1665-1731
    ISSN (online) 1665-1731
    ISSN 1665-1731
    DOI 10.24875/ACM.210003261
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  5. Article ; Online: Neurofibromatosis Type 1: Diagnostic Timelines in Children.

    García-Martínez, F J / Hernández-Martín, A

    Actas dermo-sifiliograficas

    2022  Volume 114, Issue 3, Page(s) 187–193

    Abstract: Background and objectives: The neurofibromatosis 1 (NF1) diagnosis is challenging in young children without a family history of NF1. The aims of this study were to estimate diagnostic delays in children without a family history of NF1 and to examine the ...

    Title translation Cronología del diagnóstico de la neurofibromatosis tipo 1 en la infancia.
    Abstract Background and objectives: The neurofibromatosis 1 (NF1) diagnosis is challenging in young children without a family history of NF1. The aims of this study were to estimate diagnostic delays in children without a family history of NF1 and to examine the effects of using café au lait macules and skin fold freckling as a single diagnostic criterion.
    Patients and methods: Retrospective, descriptive, observational study of all patients diagnosed with NF1 before the age of 18 years who were seen at our hospital. The medical records of those included were reviewed to identify the date on which the diagnostic criteria of NF1 were objectified. The patients were categorized into 2 groups: those with a known parental history of NF1 and those without. Café au lait macules and skin fold freckling were assessed as a single diagnostic criterion, and genetic evidence was considered to confirm highly suspicious cases.
    Results: We studied 108 patients younger than the age of 18 years with a diagnosis of NF1. Mean (SD) age at diagnosis was 3.94 (±3.8) years for the overall group, 1 year for patients with a parental history of NF1, and 4 years and 8 months for those without. Diagnosis was therefore delayed by 3 years and 8 months in patients without a family history.
    Conclusion: Skin lesions were the first clinical manifestation of NF1 in most patients. We believe that the National Institutes of Health's diagnostic criteria for NF1 should be updated to aid diagnosis in young children.
    MeSH term(s) Humans ; Child ; Child, Preschool ; Adolescent ; Neurofibromatosis 1/diagnosis ; Neurofibromatosis 1/genetics ; Neurofibromatosis 1/pathology ; Retrospective Studies ; Cafe-au-Lait Spots/diagnosis ; Skin Diseases ; Melanosis
    Language Spanish
    Publishing date 2022-11-09
    Publishing country Spain
    Document type Observational Study ; Journal Article
    ZDB-ID 390255-9
    ISSN 1578-2190 ; 0001-7310 ; 1138-8196
    ISSN (online) 1578-2190
    ISSN 0001-7310 ; 1138-8196
    DOI 10.1016/j.ad.2022.10.036
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  6. Article ; Online: Cronología del diagnóstico de la neurofibromatosis tipo 1 en la infancia

    F.J. García-Martínez / A. Hernández-Martín

    Actas Dermo-Sifiliográficas, Vol 114, Iss 3, Pp 187-

    2023  Volume 193

    Abstract: ... en las historias clínicas de los pacientes menores de 18 años atendidos en nuestro centro. Distribuimos a ... objectives: The neurofibromatosis 1 (NF1) diagnosis is challenging in young children without a family history ... of NF1. The aims of this study were to estimate diagnostic delays in children without a family ...

    Abstract Resumen: Antecedentes y objetivos: El diagnóstico de la neurofibromatosis 1 (NF1) plantea dificultades en niños sin antecedentes familiares durante la primera infancia. En este estudio pretendemos estimar la demora diagnóstica de los pacientes sin antecedentes familiares de NF1 y definir la repercusión de considerar las manchas café con leche y las efélides como un único criterio diagnóstico. Pacientes y métodos: Estudio observacional descriptivo retrospectivo en el que se revisaron los hitos diagnósticos de la NF1 en las historias clínicas de los pacientes menores de 18 años atendidos en nuestro centro. Distribuimos a los pacientes en dos grupos en función de la existencia de antecedentes de NF1 entre sus progenitores, considerando las manchas café con leche y las efélides como un único criterio y aceptando el estudio genético como criterio de confirmación en casos de elevada sospecha. Resultados: Se incluyeron en el estudio 108 menores con diagnóstico de NF1. La edad media de diagnóstico en nuestra serie fue de 3,94 años (desviación estándar: ± 3,8 años). En el grupo 1, sin antecedentes, la edad media de diagnóstico fue de 4 años y 8 meses, mientras que en el grupo 2, con antecedentes, fue de 12 meses, siendo la demora en el diagnóstico de 3 años y 8 meses entre ambos grupos. Conclusión: Las lesiones cutáneas representan, en la mayoría de los casos, las primeras manifestaciones clínicas de la enfermedad. Consideramos necesaria la actualización de los criterios diagnósticos del NIH con el fin de facilitar el diagnóstico en los primeros años de vida. Abstract: Background and objectives: The neurofibromatosis 1 (NF1) diagnosis is challenging in young children without a family history of NF1. The aims of this study were to estimate diagnostic delays in children without a family history of NF1 and to examine the effects of using café au lait macules and skin fold freckling as a single diagnostic criterion. Patients and methods: Retrospective, descriptive, observational study of all patients diagnosed with NF1 ...
    Keywords Neurofibromatosis type 1 ; Cafe-au-lait spots ; Skin fold freckling ; Nevus anemicus ; Juvenile xanthogranuloma ; Diagnostic criteria ; Dermatology ; RL1-803 ; Internal medicine ; RC31-1245
    Subject code 610
    Language English
    Publishing date 2023-03-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
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  7. Article ; Online: [Translated article] Neurofibromatosis Type 1

    F.J. García-Martínez / A. Hernández-Martín

    Actas Dermo-Sifiliográficas, Vol 114, Iss 3, Pp T187-T

    Diagnostic Timelines in Children

    2023  Volume 193

    Abstract: Background and objectives: Diagnosis of neurofibromatosis 1 (NF1) diagnosis is challenging in young children without a family history of NF1. The aims of this study were to estimate diagnostic delays in children without a family history of NF1 and to ... ...

    Abstract Background and objectives: Diagnosis of neurofibromatosis 1 (NF1) diagnosis is challenging in young children without a family history of NF1. The aims of this study were to estimate diagnostic delays in children without a family history of NF1 and to examine the effects of considering café-au-lait macules and skinfold freckling as a single diagnostic criterion. Patients and methods: Retrospective, descriptive, observational study of all patients diagnosed with NF1 before the age of 18 years who were seen at our hospital. The medical records of those included were reviewed to identify the date on which the diagnostic criteria of NF1 were objectified. The patients were categorized into 2 groups: those with a known parental history of NF1 and those without. Café-au-lait macules and skinfold freckling were assessed as a single diagnostic criterion, and genetic evidence was considered to confirm highly suspicious cases. Results: We studied 108 patients younger than the age of 18 years with a diagnosis of NF1. Mean (SD) age at diagnosis was 3.94 (±3.8) years for the overall group, 1 year for patients with a parental history of NF1, and 4 years and 8 months for those without. Diagnosis was therefore delayed by 3 years and 8 months in patients without a family history. Conclusion: Skin lesions were the first clinical manifestation of NF1 in most patients. We believe that the National Institutes of Health's diagnostic criteria for NF1 should be updated to aid diagnosis in young children. Resumen: Antecedentes y objetivos: El diagnóstico de la neurofibromatosis 1 (NF1) plantea dificultades en niños sin antecedentes familiares durante la primera infancia. En este estudio pretendemos estimar la demora diagnóstica de los pacientes sin antecedentes familiares de NF1 y definir la repercusión de considerar las manchas café con leche y las efélides como un único criterio diagnóstico. Pacientes y métodos: Estudio observacional descriptivo retrospectivo en el que se revisaron los hitos diagnósticos de la NF1 en las historias ...
    Keywords Neurofibromatosis 1 ; Manchas café con leche ; Efélides ; Nevus anémico ; Xantogranuloma juvenil ; Criterios diagnósticos ; Dermatology ; RL1-803 ; Internal medicine ; RC31-1245
    Subject code 610
    Language English
    Publishing date 2023-03-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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    Inter-library loan at ZB MED

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  8. Article ; Online: Otorhinolaryngologic anomalies in children and young adults with congenital ichthyoses and keratinization disorders: Prospective assessment in a multidisciplinary clinic.

    Santos, Saturnino / Martin-Alcalde, Javier / Hernández-Martín, Ángela

    Journal of the American Academy of Dermatology

    2021  Volume 86, Issue 6, Page(s) 1431–1433

    MeSH term(s) Child ; Humans ; Ichthyosiform Erythroderma, Congenital ; Ichthyosis ; Prospective Studies ; Skin Neoplasms ; Young Adult
    Language English
    Publishing date 2021-06-30
    Publishing country United States
    Document type Journal Article
    ZDB-ID 603641-7
    ISSN 1097-6787 ; 0190-9622
    ISSN (online) 1097-6787
    ISSN 0190-9622
    DOI 10.1016/j.jaad.2021.06.857
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    Zs.A 1540: Show issues Location:
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  9. Article ; Online: Oral Ivermectin to Treat Papulopustular Rosacea in a immunocompetent patient.

    Hernández-Martín, Á

    Actas dermo-sifiliograficas

    2017  Volume 108, Issue 7, Page(s) 685–686

    Title translation Tratamiento con ivermectina oral en un paciente inmunocompetente con rosácea pápulo-pustulosa.
    MeSH term(s) Administration, Oral ; Adult ; Humans ; Immunocompetence ; Ivermectin/administration & dosage ; Male ; Rosacea/drug therapy
    Chemical Substances Ivermectin (70288-86-7)
    Language Spanish
    Publishing date 2017-03-17
    Publishing country Spain
    Document type Case Reports ; Letter
    ZDB-ID 390255-9
    ISSN 1578-2190 ; 0001-7310 ; 1138-8196
    ISSN (online) 1578-2190
    ISSN 0001-7310 ; 1138-8196
    DOI 10.1016/j.ad.2017.01.011
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  10. Article ; Online: Reply To: The Possible Combined Action of Different Trigger Agents in Rosacea.

    Hernández-Martín, Á

    Actas dermo-sifiliograficas

    2017  Volume 109, Issue 1, Page(s) 92–93

    MeSH term(s) Dermatologic Agents ; Humans ; Rosacea
    Chemical Substances Dermatologic Agents
    Language Spanish
    Publishing date 2017-10-12
    Document type Letter ; Comment
    ZDB-ID 2541876-2
    ISSN 2173-5778 ; 2173-5778
    ISSN (online) 2173-5778
    ISSN 2173-5778
    DOI 10.1016/j.ad.2017.08.002
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