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Results 1 - 20 of 1,813  for All Library Resources

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Refined by: creation date: 1976 To 1991 remove
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1
Long-Term Outcome after Surgical Repair of Isolated Atrial Septal Defect: Follow-up at 27 to 32 Years
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Article
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Long-Term Outcome after Surgical Repair of Isolated Atrial Septal Defect: Follow-up at 27 to 32 Years

The New England journal of medicine, 1990-12, Vol.323 (24), p.1645-1650 [Peer Reviewed Journal]

1993 INIST-CNRS ;Copyright Massachusetts Medical Society Dec 13, 1990 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJM199012133232401 ;PMID: 2233961 ;CODEN: NEJMAG

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2
Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa : a consensus report by the Subcommittee on diagnosis and classification of the national epidermolysis bullosa registry
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Article
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Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa : a consensus report by the Subcommittee on diagnosis and classification of the national epidermolysis bullosa registry

Journal of the American Academy of Dermatology, 1991, Vol.24 (1), p.119-135 [Peer Reviewed Journal]

1991 INIST-CNRS ;ISSN: 0190-9622 ;EISSN: 1097-6787 ;DOI: 10.1016/0190-9622(91)70021-S ;PMID: 1999509 ;CODEN: JAADDB

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3
Neurocutaneous melanosis: Definition and review of the literature
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Article
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Neurocutaneous melanosis: Definition and review of the literature

Journal of the American Academy of Dermatology, 1991-05, Vol.24 (5), p.747-755 [Peer Reviewed Journal]

1991 American Academy of Dermatology, Inc. ;1991 INIST-CNRS ;ISSN: 0190-9622 ;EISSN: 1097-6787 ;DOI: 10.1016/0190-9622(91)70115-I ;PMID: 1869648 ;CODEN: JAADDB

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4
Maternal-Fetal Transfer of Thyroxine in Congenital Hypothyroidism Due to a Total Organification Defect or Thyroid Agenesis
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Article
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Maternal-Fetal Transfer of Thyroxine in Congenital Hypothyroidism Due to a Total Organification Defect or Thyroid Agenesis

The New England journal of medicine, 1989-07, Vol.321 (1), p.13-16 [Peer Reviewed Journal]

1990 INIST-CNRS ;Copyright Massachusetts Medical Society Jul 6, 1989 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJM198907063210103 ;PMID: 2733742 ;CODEN: NEJMAG

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5
A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome
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Article
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A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

Cell, 1990-08, Vol.62 (4), p.777-791 [Peer Reviewed Journal]

1990 ;1991 INIST-CNRS ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/0092-8674(90)90122-U ;PMID: 2167179 ;CODEN: CELLB5

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6
Right Ventricular Cardiomyopathy and Sudden Death in Young People
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Article
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Right Ventricular Cardiomyopathy and Sudden Death in Young People

The New England journal of medicine, 1988-01, Vol.318 (3), p.129-133 [Peer Reviewed Journal]

1988 INIST-CNRS ;Copyright Massachusetts Medical Society Jan 21, 1988 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJM198801213180301 ;PMID: 3336399 ;CODEN: NEJMAG

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7
Current Concepts: Transfusion-Associated Graft-versus-Host Disease
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Article
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Current Concepts: Transfusion-Associated Graft-versus-Host Disease

The New England journal of medicine, 1990-08, Vol.323 (5), p.315 [Peer Reviewed Journal]

Copyright Massachusetts Medical Society Aug 2, 1990 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJM199008023230506

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8
The Genetic Defect in Cockayne Syndrome is Associated with a Defect in Repair of UV-Induced DNA Damage in Transcriptionally Active DNA
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Article
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The Genetic Defect in Cockayne Syndrome is Associated with a Defect in Repair of UV-Induced DNA Damage in Transcriptionally Active DNA

Proceedings of the National Academy of Sciences - PNAS, 1990-06, Vol.87 (12), p.4707-4711 [Peer Reviewed Journal]

1991 INIST-CNRS ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.87.12.4707 ;PMID: 2352945 ;CODEN: PNASA6

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9
Antecedents of Cerebral Palsy
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Article
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Antecedents of Cerebral Palsy

The New England journal of medicine, 1986-07, Vol.315 (2), p.81-86 [Peer Reviewed Journal]

Copyright Massachusetts Medical Society Jul 10, 1986 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJM198607103150202

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10
Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain
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Article
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Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain

Nature (London), 1990-11, Vol.348 (6296), p.73-76 [Peer Reviewed Journal]

1991 INIST-CNRS ;Copyright Macmillan Journals Ltd. Nov 1, 1990 ;Copyright Nature Publishing Group Nov 1, 1990 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/348073a0 ;PMID: 2234061 ;CODEN: NATUAS

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11
Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation
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Article
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Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation

The Lancet (British edition), 1991-03, Vol.337 (8744), p.762-763 [Peer Reviewed Journal]

1991 ;1992 INIST-CNRS ;Copyright Lancet Ltd. Mar 30, 1991 ;Copyright Elsevier Limited Mar 30, 1991 ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/0140-6736(91)91374-4 ;PMID: 1672394 ;CODEN: LANCAO

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12
Increased Need for Thyroxine during Pregnancy in Women with Primary Hypothyroidism
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Article
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Increased Need for Thyroxine during Pregnancy in Women with Primary Hypothyroidism

The New England journal of medicine, 1990-07, Vol.323 (2), p.91-96 [Peer Reviewed Journal]

Copyright Massachusetts Medical Society Jul 12, 1990 ;Copyright Massachusetts Medical Society, Publishing Division Jul 12, 1990 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJM199007123230204 ;PMID: 2359428 ;CODEN: NEJMAG

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13
Treatment of Children with Port-Wine Stains Using the Flashlamp-Pulsed Tunable Dye Laser
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Article
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Treatment of Children with Port-Wine Stains Using the Flashlamp-Pulsed Tunable Dye Laser

The New England journal of medicine, 1989-02, Vol.320 (7), p.416-421 [Peer Reviewed Journal]

1989 INIST-CNRS ;Copyright Massachusetts Medical Society Feb 16, 1989 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJM198902163200702 ;PMID: 2913507 ;CODEN: NEJMAG

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14
Effects of Recombinant Human Granulocyte Colony-Stimulating Factor on Neutropenia in Patients with Congenital Agranulocytosis
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Article
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Effects of Recombinant Human Granulocyte Colony-Stimulating Factor on Neutropenia in Patients with Congenital Agranulocytosis

The New England journal of medicine, 1989-06, Vol.320 (24), p.1574-1580 [Peer Reviewed Journal]

1990 INIST-CNRS ;Copyright Massachusetts Medical Society Jun 15, 1989 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJM198906153202402 ;PMID: 2471075 ;CODEN: NEJMAG

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15
Xeroderma Pigmentosum Group E Cells Lack a Nuclear Factor That Binds to Damaged DNA
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Article
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Xeroderma Pigmentosum Group E Cells Lack a Nuclear Factor That Binds to Damaged DNA

Science (American Association for the Advancement of Science), 1988-10, Vol.242 (4878), p.564-567 [Peer Reviewed Journal]

Copyright 1988 The American Association for the Advancement of Science ;1989 INIST-CNRS ;COPYRIGHT 1988 American Association for the Advancement of Science ;Copyright American Association for the Advancement of Science Oct 28, 1988 ;ISSN: 0036-8075 ;EISSN: 1095-9203 ;DOI: 10.1126/science.3175673 ;PMID: 3175673 ;CODEN: SCIEAS

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16
Complementation of DNA repair in xeroderma pigmentosum group A cell extracts by a protein with affinity for damaged DNA
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Article
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Complementation of DNA repair in xeroderma pigmentosum group A cell extracts by a protein with affinity for damaged DNA

The EMBO journal, 1991-12, Vol.10 (12), p.3913-3921 [Peer Reviewed Journal]

1991 European Molecular Biology Organization ;1992 INIST-CNRS ;ISSN: 0261-4189 ;EISSN: 1460-2075 ;DOI: 10.1002/j.1460-2075.1991.tb04961.x ;PMID: 1935910 ;CODEN: EMJODG

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17
The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA
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Article
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The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA

Nucleic acids research, 1990-02, Vol.18 (3), p.443-448 [Peer Reviewed Journal]

1990 INIST-CNRS ;ISSN: 0305-1048 ;EISSN: 1362-4962 ;DOI: 10.1093/nar/18.3.443 ;PMID: 2308842 ;CODEN: NARHAD

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18
The natural history of epistaxis in hereditary hemorrhagic telangiectasia
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Article
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The natural history of epistaxis in hereditary hemorrhagic telangiectasia

The Laryngoscope, 1991-09, Vol.101 (9), p.977-980 [Peer Reviewed Journal]

Copyright © 1991 The Triological Society ;1992 INIST-CNRS ;ISSN: 0023-852X ;EISSN: 1531-4995 ;DOI: 10.1288/00005537-199109000-00008 ;PMID: 1886446 ;CODEN: LARYA8

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19
Treatment of port-wine stains during childhood with the flashlamp-pumped pulsed dye laser
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Article
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Treatment of port-wine stains during childhood with the flashlamp-pumped pulsed dye laser

Journal of the American Academy of Dermatology, 1990-12, Vol.23 (6), p.1142-1148 [Peer Reviewed Journal]

1990 American Academy of Dermatology, Inc. ;1991 INIST-CNRS ;ISSN: 0190-9622 ;EISSN: 1097-6787 ;DOI: 10.1016/0190-9622(90)70348-L ;PMID: 2273116 ;CODEN: JAADDB

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20
Congenital diseases: Complementary genes for an adrenal enzyme deficiency
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Article
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Congenital diseases: Complementary genes for an adrenal enzyme deficiency

Nature (London), 1985-03, Vol.314 (6007), p.130-131 [Peer Reviewed Journal]

ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/314130b0

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