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  1. Book: Type 2 diabetes

    Goldstein, Barry J.

    principles and practice

    2008  

    Author's details ed. by Barry J. Goldstein
    Keywords Diabetes Mellitus, Type 2 ; Non-insulin-dependent diabetes
    Subject code 616.462
    Language English
    Size XI, 591 S. : Ill., graph. Darst., 26cm
    Edition 2. ed.
    Publisher Informa Healthcare
    Publishing place New York u.a.
    Publishing country United States
    Document type Book
    Old title 1. Aufl. u.d.T. Textbook of type 2 diabetes
    HBZ-ID HT015019891
    ISBN 978-0-8493-7957-4 ; 0-8493-7957-1
    Database Catalogue ZB MED Medicine, Health

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  2. Book: Textbook of type 2 diabetes

    Goldstein, Barry J.

    2003  

    Title variant Type 2 diabetes
    Author's details ed. by Barry J. Goldstein
    Keywords Diabetes Mellitus, Non-Insulin-Dependent
    Language English
    Size XIV, 480 S. : Ill., graph. Darst.
    Publisher Dunitz
    Publishing place London u.a.
    Publishing country Great Britain
    Document type Book
    New title 2. Aufl. u.d.T. Type 2 diabetes
    HBZ-ID HT013716171
    ISBN 1-84184-109-9 ; 978-1-84184-109-0
    Database Catalogue ZB MED Medicine, Health

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  3. Book: Diabetes mellitus

    Goldstein, Barry J.

    (Clinics in laboratory medicine ; 21,1)

    2001  

    Author's details Barry J. Goldstein ..., guest ed
    Series title Clinics in laboratory medicine ; 21,1
    Collection
    Language English
    Size XII, 216 S. : Ill., graph. Darst.
    Publisher Saunders
    Publishing place Philadelphia u.a.
    Publishing country United States
    Document type Book
    HBZ-ID HT012999532
    Database Catalogue ZB MED Medicine, Health

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  4. Book ; Conference proceedings: A Symposium: Evolution of Type 2 Diabetes Mellitus Management: Assessment and Clinical Application of Newer Findings

    Goldstein, Barry J.

    ... based on a roundtable meeting held July 11 - 12, 2001, in Chicago, Illinois

    (The American journal of cardiology ; 90,5A)

    2002  

    Title variant Evolution of type 2 diabetes mellitus management
    Event/congress Symposium: Evolution of Type 2 Diabetes Mellitus Management: Assessment and Clinical Application of Newer Findings (2001, ChicagoIll.)
    Author's details guest. ed.: Barry J. Goldstein
    Series title The American journal of cardiology ; 90,5A
    Collection
    Language English
    Size 50G S. : Ill., graph. Darst.
    Publisher Excerpta Medica
    Publishing place New York, NY
    Publishing country United States
    Document type Book ; Conference proceedings
    HBZ-ID HT013460045
    Database Catalogue ZB MED Medicine, Health

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  5. Book: Tyrosine phosphoprotein phosphatases

    Goldstein, Barry J.

    (Protein profile)

    1998  

    Author's details Barry J. Goldstein
    Series title Protein profile
    Keywords Phosphoproteinphosphatase ; Tyrosin
    Subject Proteinphosphatase ; EC 3.1.3.16 ; Serin ; Proteinphosphatase-1 ; Proteinphosphatase-2A ; Proteinphosphatase-2B ; Proteinphosphatase-2C
    Language English
    Size XI, 260 S. : Ill.
    Edition 2. ed.
    Publisher Oxford Univ. Press
    Publishing place Oxford u.a.
    Publishing country Great Britain
    Document type Book
    HBZ-ID HT008806142
    ISBN 0-19-850247-8 ; 978-0-19-850247-0
    Database Catalogue ZB MED Medicine, Health

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  6. Article ; Online: Should We Call It a Prostate? A Review of the Female Periurethral Glandular Tissue Morphology, Histochemistry, Nomenclature, and Role in Iatrogenic Sexual Dysfunction.

    Tomalty, Diane / Giovannetti, Olivia / Hannan, Johanna / Komisaruk, Barry / Goldstein, Sue / Goldstein, Irwin / Adams, Michael

    Sexual medicine reviews

    2022  Volume 10, Issue 2, Page(s) 183–194

    Abstract: ... involved in the FSR, and its role in FSD following surgical injury. Tomalty D, Giovannetti O, Hannan J, et ...

    Abstract Introduction: There is evidence of glandular tissue within the region of the anterior vaginal wall-female periurethral tissue (AVW-FPT) having similar morphology and immunohistochemistry to the prostate in men and having physiological roles in the female sexual response (FSR). Whether this tissue should be called a prostate in women has been debated. Iatrogenic injury to structures of the AVW-FPT, including these glands and the associated neurovasculature, could be a cause of female sexual dysfunction (FSD).
    Objectives: To consolidate the current knowledge concerning the glandular tissue surrounding the urethra in women, evidence was reviewed to address whether: (i) these glands comprise the prostate in women, (ii) they have specific functions in the FSR, and (iii) injury to the AVW-FPT and prostate has sexual dysfunction as a likely outcome.
    Methods: A literature review was conducted using keywords including female prostate, Skene's/paraurethral glands, periurethral tissue, Gräfenberg (G)-spot, female ejaculation, mid-urethral sling (MUS), and sexual dysfunction.
    Results: Histological and immunohistochemical studies of the glandular tissue surrounding the urethra support the existence of prostate in women. Evidence suggests this tissue may have physiologically and clinically relevant autonomic and sensory innervation, and during sexual arousal may contribute to secretions involved in ejaculation and orgasm. Gaps in knowledge relating to the functional anatomy, physiological roles, and embryological origins of this tissue have impeded the acceptance of a prostate in women. Injury to the innervation, vasculature, and/or glandular tissue within the surgical field of MUS implantation suggests iatrogenic sexual dysfunction is plausible.
    Conclusions: Continuing to advance our understanding of the morphology, histochemistry, and physiologic capacity of this glandular tissue will clarify the characterization of this tissue as the "prostate" involved in the FSR, and its role in FSD following surgical injury. Tomalty D, Giovannetti O, Hannan J, et al. Should We Call It a Prostate? A Review of the Female Periurethral Glandular Tissue Morphology, Histochemistry, Nomenclature, and Role in Iatrogenic Sexual Dysfunction. Sex Med Rev 2022;10:183-194.
    MeSH term(s) Female ; Humans ; Iatrogenic Disease ; Male ; Orgasm/physiology ; Prostate ; Suburethral Slings ; Urethra
    Language English
    Publishing date 2022-01-21
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 2722257-3
    ISSN 2050-0521 ; 2050-0513
    ISSN (online) 2050-0521
    ISSN 2050-0513
    DOI 10.1016/j.sxmr.2021.12.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Oral lasofoxifene's effects on moderate to severe vaginal atrophy in postmenopausal women: two phase 3, randomized, controlled trials.

    Kagan, Risa / Simon, James A / Goldstein, Steven R / Komm, Barry S / Jenkins, Simon N / Portman, David J

    Menopause (New York, N.Y.)

    2024  

    Abstract: Objective: The aim of this study was to demonstrate whether lasofoxifene improves vaginal signs/symptoms of genitourinary syndrome of menopause.: Methods: Two identical, phase 3 trials randomized postmenopausal women with moderate to severe vaginal ... ...

    Abstract Objective: The aim of this study was to demonstrate whether lasofoxifene improves vaginal signs/symptoms of genitourinary syndrome of menopause.
    Methods: Two identical, phase 3 trials randomized postmenopausal women with moderate to severe vaginal symptoms to oral lasofoxifene 0.25 or 0.5 mg/d, or placebo, for 12 week. Changes from baseline to week 12 in most bothersome symptom, vaginal pH, and percentages of vaginal parabasal and superficial cells were evaluated. These coprimary endpoints were analyzed using analysis of covariance, except superficial cells, which were analyzed by the nonparametric, rank-based Kruskal-Wallis test.
    Results: The two studies enrolled 444 and 445 women (mean age, ~60 y), respectively. Coprimary endpoints at week 12 improved with lasofoxifene 0.25 and 0.5 mg/d greater than with placebo (P < 0.0125 for all). Study 1: most bothersome symptom (least square mean difference from placebo: -0.4 and -0.5 for 0.25 and 0.5 mg/d, respectively), vaginal pH (-0.65, -0.58), and vaginal superficial (5.2%, 5.4%), and parabasal (-39.9%, -34.9%) cells; study 2: most bothersome symptom (-0.4, -0.5), vaginal pH (-0.57, -0.67), and vaginal superficial (3.5%, 2.2%) and parabasal (-34.1%, -33.5%) cells. Some improvements occurred as early as week 2. Most treatment-emergent adverse events were mild or moderate and hot flushes were most frequently reported (lasofoxifene vs placebo: 13%-23% vs 9%-11%). Serious adverse events were infrequent and no deaths occurred.
    Conclusions: In two phase 3 trials, oral lasofoxifene 0.25 and 0.5 mg/d provided significant and clinically meaningful improvements in vaginal signs/symptoms with a favorable safety profile, suggesting beneficial effects of lasofoxifene on genitourinary syndrome of menopause.
    Language English
    Publishing date 2024-04-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1205262-0
    ISSN 1530-0374 ; 1072-3714
    ISSN (online) 1530-0374
    ISSN 1072-3714
    DOI 10.1097/GME.0000000000002355
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Journal’s withdrawal of article. Concerns about methods used.

    Goldstein, Barry J

    BMJ (Clinical research ed.)

    2011  Volume 342, Page(s) d2722

    MeSH term(s) Gastroenterology ; Periodicals as Topic ; Retraction of Publication as Topic
    Language English
    Publishing date 2011-05-10
    Publishing country England
    Document type Comment ; Letter
    ZDB-ID 1362901-3
    ISSN 1756-1833 ; 0959-8154 ; 0959-8146 ; 0959-8138 ; 0959-535X ; 1759-2151
    ISSN (online) 1756-1833
    ISSN 0959-8154 ; 0959-8146 ; 0959-8138 ; 0959-535X ; 1759-2151
    DOI 10.1136/bmj.d2722
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Addiction in focus: molecular mechanisms, model systems, circuit maps, risk prediction and the quest for effective interventions.

    Goldstein, Rita Z / Barrot, Michel / Everitt, Barry J / Foxe, John J

    The European journal of neuroscience

    2019  Volume 50, Issue 3, Page(s) 2007–2013

    MeSH term(s) Brain/drug effects ; Brain/physiopathology ; Humans ; Models, Biological ; Research Design ; Risk Assessment ; Substance-Related Disorders/drug therapy ; Substance-Related Disorders/physiopathology
    Language English
    Publishing date 2019-09-06
    Publishing country France
    Document type Editorial
    ZDB-ID 645180-9
    ISSN 1460-9568 ; 0953-816X
    ISSN (online) 1460-9568
    ISSN 0953-816X
    DOI 10.1111/ejn.14544
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Catheterization for Congenital Heart Disease Adjustment for Risk Method II.

    Quinn, Brian P / Gunnelson, Lauren C / Kotin, Sarah G / Gauvreau, Kimberlee / Yeh, Mary J / Hasan, Babar / Lozier, John / Barry, Oliver M / Shahanavaz, Shabana / Batlivala, Sarosh P / Salavitabar, Arash / Foerster, Susan / Goldstein, Bryan / Divekar, Abhay / Holzer, Ralf / Nicholson, George T / O'Byrne, Michael L / Whiteside, Wendy / Bergersen, Lisa

    Circulation. Cardiovascular interventions

    2024  Volume 17, Issue 3, Page(s) e012834

    Abstract: Background: Current metrics used to adjust for case mix complexity in congenital cardiac catheterization are becoming outdated due to the introduction of novel procedures, innovative technologies, and expanding patient subgroups. This study aims to ... ...

    Abstract Background: Current metrics used to adjust for case mix complexity in congenital cardiac catheterization are becoming outdated due to the introduction of novel procedures, innovative technologies, and expanding patient subgroups. This study aims to develop a risk adjustment methodology introducing a novel, clinically meaningful adverse event outcome and incorporating a modern understanding of risk.
    Methods: Data from diagnostic only and interventional cases with defined case types were collected for patients ≤18 years of age and ≥2.5 kg at all Congenital Cardiac Catheterization Project on Outcomes participating centers. The derivation data set consisted of cases performed from 2014 to 2017, and the validation data set consisted of cases performed from 2019 to 2020. Severity level 3 adverse events were stratified into 3 tiers by clinical impact (3a/b/c); the study outcome was clinically meaningful adverse events, severity level ≥3b (3bc/4/5).
    Results: The derivation data set contained 15 224 cases, and the validation data set included 9462 cases. Clinically meaningful adverse event rates were 4.5% and 4.2% in the derivation and validation cohorts, respectively. The final risk adjustment model included age <30 days, Procedural Risk in Congenital Cardiac Catheterization risk category, and hemodynamic vulnerability score (C statistic, 0.70; Hosmer-Lemeshow
    Conclusions: CHARM II (Congenital Heart Disease Adjustment for Risk Method II) risk adjustment methodology allows for equitable comparison of clinically meaningful adverse events among institutions and operators with varying patient populations and case mix complexity performing pediatric cardiac catheterization.
    MeSH term(s) Child ; Humans ; Infant ; Risk Factors ; Treatment Outcome ; Cardiac Catheterization/adverse effects ; Cardiac Catheterization/methods ; Heart Defects, Congenital/diagnosis ; Heart Defects, Congenital/therapy ; Hemodynamics ; Risk Adjustment/methods
    Language English
    Publishing date 2024-01-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2450797-0
    ISSN 1941-7632 ; 1941-7640
    ISSN (online) 1941-7632
    ISSN 1941-7640
    DOI 10.1161/CIRCINTERVENTIONS.123.012834
    Database MEDical Literature Analysis and Retrieval System OnLINE

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