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  1. Book ; Online: Schutzgebiete vor Pestiziden schützen

    Smolka, Susanne / Gripp, Tamara

    eine gesunde Welt für alle, Mensch und Umwelt vor Pestiziden schützen, Alternativen fördern

    2019  

    Author's details Text: Susanne Smolka & Tamara Gripp
    Language German
    Size 1 Online-Ressource (12 Seiten), Illustrationen, Diagramme, Karten
    Publisher Pestizid Aktions-Netzwerk e.V. (PAN Germany)
    Publishing place Hamburg
    Publishing country Germany
    Document type Book ; Online
    Note Open Access
    HBZ-ID HT021010660
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

    Full text online

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  2. Article: Validity of S-100 B in patients after brain radiation.

    Gripp, S / Peiper, M / Matuschek, C / Giro, C / Steinbach, G / Hermsen, D / van Griensven, M / Budach, W / Engers, R / Gerber, P A / Hefter, H / Spiess, B / Orth, K / Bölke, E

    European journal of medical research

    2008  Volume 13, Issue 6, Page(s) 299–303

    Abstract: Background: S-100B is a calcium binding acute phase protein and a potential biomarker ... for brain injury. In prior studies elevated plasma S-100B levels were detected in stroke and severe head trauma ... The aim of this study was to evaluate whether S-100 B is elevated during cerebral radiotherapy and ...

    Abstract Background: S-100B is a calcium binding acute phase protein and a potential biomarker for brain injury. In prior studies elevated plasma S-100B levels were detected in stroke and severe head trauma. The aim of this study was to evaluate whether S-100 B is elevated during cerebral radiotherapy and whether that is associated with adverse outcomes.
    Material and methods: In this prospective pilot study, 45 patients (25 males, 20 females, median age 58 (17-81)) underwent cerebral radiation therapy because of a primary or metastaic cerebral malignancy. 39 patients were included in the evaluation. 6 patients died during the study period. S-100 plasma concentrations were measured with an electrochemiluminescence immunoassay on admission and weekly during radiation therapy for the duration of 6 weeks. In 10 healthy young volunteers (5 males, 5 females, median age 32 (28-36)) S-100 B plasma levels were measured weekly for 6 weeks as a negative control. Furthermore, in an active control 10 patients (4 males, 6 females, median age 68 (64-76)) with stroke (7 = major stroke, 3 = lacunar infarct) S- 100 B plasma levels were measured for 7 consecutive days after the event.
    Results: During radiotherapy S-100 B plasma concentrations increased from median baseline values of 0.030 microg/l to 0.044 microg/l. For the time of radiation therapy most patients showed a mild increase, but absolute plasma values were still within the normal range. In the control group of healthy volunteers S-100 B remained unchanged. In stroke patients S-100 B increased to maximum values of 1.7 microg/l three days after the event. In the 3 patients with lacunar infarcts no increase of S-100 B levels could be detected.
    Conclusion: Brain irradiation leads to a mild increase of S-100 B plasma levels. However, the absolute rise was far weaker compared to that seen in major brain injuries.
    MeSH term(s) Adolescent ; Adult ; Aged ; Aged, 80 and over ; Biomarkers/metabolism ; Brain/diagnostic imaging ; Brain/metabolism ; Female ; Gene Expression Regulation ; Humans ; Male ; Middle Aged ; Nerve Growth Factors/biosynthesis ; Pilot Projects ; Prospective Studies ; Radiography ; Radiotherapy/methods ; S100 Calcium Binding Protein beta Subunit ; S100 Proteins/biosynthesis
    Chemical Substances Biomarkers ; Nerve Growth Factors ; S100 Calcium Binding Protein beta Subunit ; S100 Proteins
    Language English
    Publishing date 2008-06-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 1329381-3
    ISSN 2047-783X ; 0949-2321
    ISSN (online) 2047-783X
    ISSN 0949-2321
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    Zs.A 4636: Show issues Location:
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  3. Book ; Thesis: Glasfasern in der klinischen Dosimetrie

    Gripp, Stephan

    2000  

    Author's details vorgelegt von Stephan Gripp
    Language English ; German
    Size Getr. Zählung
    Publishing country Germany
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Düsseldorf, Univ., Habil.-Schr., 2000
    Note Beitr. teilw. dt., engl. ; Ursprünglich als Zeitschriftenaufsätze erschienen
    HBZ-ID HT013427928
    Database Catalogue ZB MED Medicine, Health

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    2003 E 189 order to use in reading room Magazin

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  4. Article: Current recommendations for management of paediatric diabetic ketoacidosis.

    Gripp, Karen E / Trottier, Evelyne D / Thakore, Sidd / Sniderman, Jonathan / Lawrence, Sarah

    Paediatrics & child health

    2023  Volume 28, Issue 2, Page(s) 128–138

    Abstract: Treatment of paediatric diabetic ketoacidosis (DKA) includes careful attention to fluids and electrolytes to minimize the risk of complications such as cerebral injury (CI), which is associated with high morbidity and mortality. The incidence of cerebral ...

    Abstract Treatment of paediatric diabetic ketoacidosis (DKA) includes careful attention to fluids and electrolytes to minimize the risk of complications such as cerebral injury (CI), which is associated with high morbidity and mortality. The incidence of cerebral edema in paediatric DKA has not decreased despite the use of fluid-limiting protocols based on restricting early fluid resuscitation. New evidence suggests that early isotonic fluid therapy does not confer additional risk and may improve outcomes in some patients. Protocols and clinical practice guidelines are being adjusted, with a particular focus on recommendations for initial and ongoing fluids and electrolyte monitoring and replacement. Initial isotonic fluid resuscitation is now recommended for all patients in the first 20 to 30 minutes after presentation, followed by repletion of volume deficit over 36 hours in association with an insulin infusion, electrolyte supplementation, and careful monitoring for and management of potential CI.
    Language English
    Publishing date 2023-05-04
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 2106767-3
    ISSN 1918-1485 ; 1205-7088
    ISSN (online) 1918-1485
    ISSN 1205-7088
    DOI 10.1093/pch/pxac119
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    Zs.A 5774: Show issues Location:
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  5. Article: Les recommandations en vigueur pour la prise en charge de l'acidocétose diabétique pédiatrique.

    Gripp, Karen E / Trottier, Evelyne D / Thakore, Sidd / Sniderman, Jonathan / Lawrence, Sarah

    Paediatrics & child health

    2023  Volume 28, Issue 2, Page(s) 128–138

    Abstract: Pour traiter l'acidocétose diabétique pédiatrique, il faut porter une attention particulière aux liquides et aux électrolytes pour limiter le risque de complications, telles qu'une lésion cérébrale, associée à une morbidité et une mortalité élevées. L' ... ...

    Abstract Pour traiter l'acidocétose diabétique pédiatrique, il faut porter une attention particulière aux liquides et aux électrolytes pour limiter le risque de complications, telles qu'une lésion cérébrale, associée à une morbidité et une mortalité élevées. L'incidence d'œdème cérébral en cas d'acidocétose diabétique n'a pas diminué malgré les protocoles visant la limitation des liquides qui s'appuient sur la restriction de la réanimation liquidienne initiale. Selon de nouvelles données probantes, l'administration précoce de liquides isotoniques n'entraîne pas de risque supplémentaire et peut améliorer les résultats cliniques chez certains patients. Les protocoles et les directives cliniques sont adaptés et axés particulièrement sur la surveillance et le remplacement initiaux et continus des liquides et des électrolytes. Il est maintenant recommandé de commencer par une réanimation à l'aide de liquides isotoniques chez tous les patients dans les 20 à 30 minutes suivant leur arrivée à l'hôpital, suivie par la réplétion du déficit volumique sur une période de 36 heures, en association avec une perfusion d'insuline et des suppléments d'électrolytes, ainsi qu'avec la surveillance et la prise en charge attentives d'une éventuelle lésion cérébrale.
    Language English
    Publishing date 2023-05-04
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 2106767-3
    ISSN 1918-1485 ; 1205-7088
    ISSN (online) 1918-1485
    ISSN 1205-7088
    DOI 10.1093/pch/pxac120
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Hemangiopericytoma: Conducts and perioperative management of an extent sinonasal tumor in a Jehovah's Witnesses patient - Case report.

    Amorim Filho, Francisco S / Gripp, Flávio M / Faria, Guilherme S / Capuzzo Gonçalves, Mateus / Miyahira, Lincoln

    Cancer reports (Hoboken, N.J.)

    2022  Volume 5, Issue 9, Page(s) e1609

    Abstract: Background: Hemangiopericytomas (HPCs) are rare tumors derived from mesenchymal cells with pericyte differentiation. About 5% of head and neck HPCs occur in the nasal cavity and paranasal sinuses. Due to its rarity, rich vascularity and variable ... ...

    Abstract Background: Hemangiopericytomas (HPCs) are rare tumors derived from mesenchymal cells with pericyte differentiation. About 5% of head and neck HPCs occur in the nasal cavity and paranasal sinuses. Due to its rarity, rich vascularity and variable biological behavior, its management is a challenge in itself.
    Case: We report a case of sinonasal HPC in a Jehovah's Witness patient and discuss the obstacles and care related to the restrictions and therapeutic challenges involved in the approach to the patient. The patient was successfully treated by endoscopic endonasal approach with all per-operative care and restrictions being respected and attended.
    Conclusions: The management of HPC by itself involves challenges and when associated with other restrictive conditions attention and care are required.
    MeSH term(s) Blood Transfusion ; Hemangiopericytoma/diagnosis ; Hemangiopericytoma/surgery ; Humans ; Jehovah's Witnesses ; Perioperative Care
    Language English
    Publishing date 2022-02-23
    Publishing country United States
    Document type Case Reports
    ISSN 2573-8348
    ISSN (online) 2573-8348
    DOI 10.1002/cnr2.1609
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  7. Book ; Thesis: Untersuchung der Luftaktivierung durch medizinisch genutzte Beschleuniger mittels Messungen an Luft-, Imidazol- und Harnstoffproben

    Gripp, Stephan

    1988  

    Size 48 S. : graph. Darst.
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Aachen, Techn. Hochsch., Diss., 1988
    HBZ-ID HT003388041
    Database Catalogue ZB MED Medicine, Health

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    Shelf markLoan statusLocation
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  8. Article: A Comparison of Lumbar Spine and Lateral Distal Femur Bone Density in Girls With Rett Syndrome.

    Gripp, Emily W / Harcke, H Theodore / Bachrach, Steven J / Kecskemethy, Heidi H

    Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry

    2020  Volume 24, Issue 3, Page(s) 374–382

    Abstract: ... Method Eleven girls (mean age 8.4 yr) with molecularly diagnosed RS and clinical DXA scan(s) were ...

    Abstract Introduction/background: Patients with Rett syndrome (RS) are at risk for low bone mineral density (BMD) and femoral fractures. In patients with RS, assessment with lateral distal femur (LDF) dual-energy X-ray absorptiometry (DXA) is recommended and clinically relevant. This study is the first to assess LDF BMD in girls with RS, and to compare LDF BMD results with lumbar spine BMD results in RS. Method Eleven girls (mean age 8.4 yr) with molecularly diagnosed RS and clinical DXA scan(s) were identified; medical charts were retrospectively reviewed. Baseline and serial lumbar spine and LDF BMD Z-scores were evaluated based on patients' ambulation status, presence of epilepsy, and mutation type. Results At the time of first scan, 8 of 11 patients had normal lumbar spine BMD and low LDF BMD Z-scores. Two patients had fracture history. Fully ambulatory (3) patients had higher lumbar spine and LDF BMD than partially (5) and nonambulatory (3) patients. Patients with epilepsy had lower average BMD at all sites. No difference was seen in lumbar spine or LDF BMD in patients with high-risk BMD mutations. Seven patients had serial DXA scans with an average observation of 5.1 yr (range 3.1 yr to 6.2 yr). Lumbar spine BMD over time was variable, while LDF bone mass accrual occurred at a lower rate than typically developing girls. Conclusion Females with RS exhibited lower BMD Z-scores at the LDF than at the lumbar spine. LDF and lumbar spine results were discordant. Ambulatory status and the presence of epilepsy were related to BMD. LDF BMD accrual deviated from normal as patients aged.
    MeSH term(s) Absorptiometry, Photon ; Aged ; Bone Density ; Child ; Female ; Femur/diagnostic imaging ; Humans ; Lumbar Vertebrae/diagnostic imaging ; Retrospective Studies ; Rett Syndrome/diagnostic imaging ; Rett Syndrome/genetics
    Language English
    Publishing date 2020-10-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2040951-5
    ISSN 1094-6950
    ISSN 1094-6950
    DOI 10.1016/j.jocd.2020.10.011
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    Zs.A 5425: Show issues Location:
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  9. Article ; Online: Comedonic lupus, a rare variant of chronic cutaneous lupus erythematosus (CCLE): case series and literature review.

    da Silveira, Camila S C / Lemos, Thayane B / Curty, Erica R G / Sampaio, Ana Luisa / Alves, Maria de Fátima G S / Antelo, Daniela A P / Gripp, Alexandre C / Azulay-Abulafia, Luna

    International journal of dermatology

    2023  Volume 62, Issue 7, Page(s) 924–932

    Abstract: Background: Cutaneous lupus erythematosus (CLE) is an autoimmune disease with several clinical presentations. The chronic form predominantly presents as discoid rashes but may present with less common morphological findings that can sometimes make ... ...

    Abstract Background: Cutaneous lupus erythematosus (CLE) is an autoimmune disease with several clinical presentations. The chronic form predominantly presents as discoid rashes but may present with less common morphological findings that can sometimes make diagnosis difficult. Comedonic lupus is a rare and underdiagnosed variant, with unknown etiology and still poorly defined treatment.
    Methods: The report illustrates a series of five cases of patients diagnosed with comedonic lupus, and it reviews 18 cases previously published in the literature.
    Results: The clinical presentation is of comedonal lesions, mostly located on the face, making a differential diagnosis with other benign conditions such as acne vulgaris, Favre-Racouchot syndrome, and syringoma, emphasizing the importance of clinical practice and histopathology for diagnostic confirmation.
    Conclusions: There is scarcity in the literature regarding the condition and therapeutic possibilities for these cases of comedonic lupus.
    MeSH term(s) Humans ; Lupus Erythematosus, Discoid/diagnosis ; Lupus Erythematosus, Cutaneous/diagnosis ; Acne Vulgaris
    Language English
    Publishing date 2023-04-18
    Publishing country England
    Document type Review ; Journal Article
    ZDB-ID 412254-9
    ISSN 1365-4632 ; 0011-9059 ; 1461-1244
    ISSN (online) 1365-4632
    ISSN 0011-9059 ; 1461-1244
    DOI 10.1111/ijd.16675
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  10. Article ; Online: HRAS

    Rodríguez, Nelson A / Patel, Nihir / Dariolli, Rafael / Ng, Simon / Aleman, Angelika G / Gong, Jingqi Q X / Lin, Hung-Mo / Rodríguez, Matthew / Josowitz, Rebecca / Sol-Church, Katia / Gripp, Karen W / Lin, Xianming / Song, Soomin C / Fishman, Glenn I / Sobie, Eric A / Gelb, Bruce D

    Circulation. Arrhythmia and electrophysiology

    2024  Volume 17, Issue 4, Page(s) e012022

    Abstract: Background: Germline : Methods: HRAS: Results: ACMs harboring : Conclusions: CS-associated gain-of- ... ...

    Abstract Background: Germline
    Methods: HRAS
    Results: ACMs harboring
    Conclusions: CS-associated gain-of-function
    MeSH term(s) Humans ; Child, Preschool ; Myocytes, Cardiac/metabolism ; Calcium/metabolism ; Heart Atria/metabolism ; Tachycardia ; Calcium Channels/metabolism ; Induced Pluripotent Stem Cells/metabolism ; Action Potentials/physiology ; Cell Differentiation ; Proto-Oncogene Proteins p21(ras)/genetics ; Proto-Oncogene Proteins p21(ras)/metabolism
    Chemical Substances Calcium (SY7Q814VUP) ; Calcium Channels ; HRAS protein, human (EC 3.6.5.2) ; Proto-Oncogene Proteins p21(ras) (EC 3.6.5.2)
    Language English
    Publishing date 2024-02-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2426129-4
    ISSN 1941-3084 ; 1941-3149
    ISSN (online) 1941-3084
    ISSN 1941-3149
    DOI 10.1161/CIRCEP.123.012022
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