Genetics Home Reference: biotin-thiamine-responsive basal ganglia disease
http://ghr.nlm.nih.gov/condition/biotin-thiamine-responsive-basal-ganglia-disease (Source: NLM General Announcements)
Source: NLM General Announcements - January 23, 2014 Category: Databases & Libraries Source Type: news

Genetics Home Reference: autosomal recessive congenital stationary night blindness
http://ghr.nlm.nih.gov/condition/autosomal-recessive-congenital-stationary-night-blindness (Source: NLM General Announcements)
Source: NLM General Announcements - January 23, 2014 Category: Databases & Libraries Source Type: news

Michael E. DeBakey Award Nominations due February 21, 2014
The Michael E. DeBakey Library Services Outreach Award for outstanding service to rural or underserved communities was established by the Friends of the National Library of Medicine (FNLM) to recognize the contributions to medical education and librarianship by Michael E. DeBakey and to honor a practicing health sciences librarian who serves such a community. The deadline for nominations is February 21. Please submit nominations by email to Ronica Lu or via fax to 301.657.1296. (Source: NLM General Announcements)
Source: NLM General Announcements - January 14, 2014 Category: Databases & Libraries Source Type: news

Genetics Home Reference: Peters anomaly
http://ghr.nlm.nih.gov/condition/peters-anomaly (Source: NLM General Announcements)
Source: NLM General Announcements - January 14, 2014 Category: Databases & Libraries Source Type: news

Genetics Home Reference: Adams-Oliver syndrome
http://ghr.nlm.nih.gov/condition/adams-oliver-syndrome (Source: NLM General Announcements)
Source: NLM General Announcements - January 14, 2014 Category: Databases & Libraries Source Type: news

Genetics Home Reference: glycogen storage disease type 0
http://ghr.nlm.nih.gov/condition/glycogen-storage-disease-type-0 (Source: NLM General Announcements)
Source: NLM General Announcements - January 7, 2014 Category: Databases & Libraries Source Type: news

Genetics Home Reference: cytogenetically normal acute myeloid leukemia
http://ghr.nlm.nih.gov/condition/cytogenetically-normal-acute-myeloid-leukemia (Source: NLM General Announcements)
Source: NLM General Announcements - January 7, 2014 Category: Databases & Libraries Source Type: news

MedlinePlus: Hipertiroidismo
(Source: NLM General Announcements)
Source: NLM General Announcements - January 3, 2014 Category: Databases & Libraries Source Type: news

MedlinePlus: Hipotiroidismo
(Source: NLM General Announcements)
Source: NLM General Announcements - January 3, 2014 Category: Databases & Libraries Source Type: news

FAQ -- DOCLINE recommended browser settings
New DOCLINE FAQ about configuring supported browsers (Source: NLM General Announcements)
Source: NLM General Announcements - December 27, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: Winchester syndrome
http://ghr.nlm.nih.gov/condition/winchester-syndrome (Source: NLM General Announcements)
Source: NLM General Announcements - December 24, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: spondyloenchondrodysplasia with immune dysregulation
http://ghr.nlm.nih.gov/condition/spondyloenchondrodysplasia-with-immune-dysregulation (Source: NLM General Announcements)
Source: NLM General Announcements - December 24, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: preeclampsia
http://ghr.nlm.nih.gov/condition/preeclampsia (Source: NLM General Announcements)
Source: NLM General Announcements - December 24, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: glucose phosphate isomerase deficiency
http://ghr.nlm.nih.gov/condition/glucose-phosphate-isomerase-deficiency (Source: NLM General Announcements)
Source: NLM General Announcements - December 24, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: FOXG1 syndrome
http://ghr.nlm.nih.gov/condition/foxg1-syndrome (Source: NLM General Announcements)
Source: NLM General Announcements - December 24, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: congenital leptin deficiency
http://ghr.nlm.nih.gov/condition/congenital-leptin-deficiency (Source: NLM General Announcements)
Source: NLM General Announcements - December 24, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: alpha-methylacyl-CoA racemase deficiency
http://ghr.nlm.nih.gov/condition/alpha-methylacyl-coa-racemase-deficiency (Source: NLM General Announcements)
Source: NLM General Announcements - December 24, 2013 Category: Databases & Libraries Source Type: news

MedlinePlus: Hyperthyroidism
(Source: NLM General Announcements)
Source: NLM General Announcements - December 24, 2013 Category: Databases & Libraries Source Type: news

MedlinePlus: Hypothyroidism
(Source: NLM General Announcements)
Source: NLM General Announcements - December 24, 2013 Category: Databases & Libraries Source Type: news

Convergent Medical Terminology (CMT) Release Files
Current Terminology Subsets Data Files. The files include 2830 new concepts that Kaiser Permanente uses for Primary Care problem lists. (Source: NLM General Announcements)
Source: NLM General Announcements - December 19, 2013 Category: Databases & Libraries Authors: Susan Roy Source Type: news

NLM Releases Digitized Collection of Its Publications and Productions
The National Library of Medicine (NLM) is pleased to announce a new addition to its Digital Collections: over 400 NLM publications and productions dating from the 1860s to the 1990s. (Source: NLM General Announcements)
Source: NLM General Announcements - December 18, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay
http://ghr.nlm.nih.gov/condition/short-stature-hyperextensibility-hernia-ocular-depression-rieger-anomaly-and-teething-delay (Source: NLM General Announcements)
Source: NLM General Announcements - December 17, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: familial dilated cardiomyopathy
http://ghr.nlm.nih.gov/condition/familial-dilated-cardiomyopathy (Source: NLM General Announcements)
Source: NLM General Announcements - December 17, 2013 Category: Databases & Libraries Source Type: news

National Library of Medicine Announces Addition of Sir William Osler Papers to Profiles in Science
Sir William Osler (1849–1919) was the best-known physician of his era. Today, he is recognized as one of the founders of modern science-based medicine. Born to Anglican missionaries in the Canadian frontier territory north of Toronto, Ontario, Osler was inspired to pursue a medical career by two early mentors, a clergyman and a physician who introduced him to natural science and to humanistic literature. When he began his training in 1868, few American medical schools included courses in laboratory sciences or required that students work with actual patients; standards of medical practice were often loose, and physic...
Source: NLM General Announcements - December 11, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: spinal muscular atrophy with progressive myoclonic epilepsy
http://ghr.nlm.nih.gov/condition/spinal-muscular-atrophy-with-progressive-myoclonic-epilepsy (Source: NLM General Announcements)
Source: NLM General Announcements - December 10, 2013 Category: Databases & Libraries Source Type: news

MedlinePlus: Seguridad sobre el uso de equipos médicos
MedlinePlus: Seguridad sobre el uso de equipos médicos (Source: NLM General Announcements)
Source: NLM General Announcements - December 6, 2013 Category: Databases & Libraries Source Type: news

WISER for Windows 4.5 is Now Available
The National Library of Medicine's WISER for Windows 4.5 is now available.  This new version of WISER fully integrates Chemical Hazards Emergency Medical Management (CHEMM) content and updates the Emergency Response Guidebook (ERG) content to 2012. (Source: NLM General Announcements)
Source: NLM General Announcements - November 27, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: multicentric osteolysis, nodulosis, and arthropathy
New Topics on Genetics Home Reference (Source: NLM General Announcements)
Source: NLM General Announcements - November 19, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: autosomal dominant congenital stationary night blindness
New Topics on Genetics Home Reference (Source: NLM General Announcements)
Source: NLM General Announcements - November 19, 2013 Category: Databases & Libraries Source Type: news

NLM Releases Enhancements to Its "Digital Collections" Repository
The National Library of Medicine, the world's largest medical library and a component of the National Institutes of Health, released several enhancements to Digital Collections, the free online archive of biomedical resources, at the end of September.  (Source: NLM General Announcements)
Source: NLM General Announcements - November 18, 2013 Category: Databases & Libraries Source Type: news

New display: DNA to Beer: Harnessing Nature in Medicine and Industry
NLM, in cooperation with the Smithsonian's National Museum of American History, launch a special display November 18, 2013: From DNA to Beer: Harnessing Nature in Medicine and Industry. (Source: NLM General Announcements)
Source: NLM General Announcements - November 15, 2013 Category: Databases & Libraries Authors: publicinfo at nlm.nih.gov Source Type: news

National Library of Medicine Launches Emergency Access Initiative, Granting Free Access to Books and Journals for Those Responding to Typhoon Haiyanin
The National Library of Medicine (NLM) Emergency Access Initiative (EAI) has been activated in support of medical efforts in the Philippines and surrounding area following the devastating typhoon. The EAI is a collaborative partnership between NLM and participating publishers to provide free access to full-text from over 650 biomedical journals and over 4,000 reference books and online databases to healthcare professionals and libraries affected by disasters. It serves as a temporary collection replacement and/or supplement for libraries affected by disasters that need to continue to serve medical staff and affiliated...
Source: NLM General Announcements - November 12, 2013 Category: Databases & Libraries Source Type: news

MedlinePlus: Trasplante de células de los islotes
MedlinePlus: Trasplante de células de los islotes (Source: NLM General Announcements)
Source: NLM General Announcements - November 8, 2013 Category: Databases & Libraries Source Type: news

National Center for Biotechnology Information Celebrates 25th Anniversary
NCBI Director Dr. David Lipman Receives Jim Gray eScience Award for Center's Accomplishments (Source: NLM General Announcements)
Source: NLM General Announcements - November 5, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: restless legs syndrome
(Source: NLM General Announcements)
Source: NLM General Announcements - November 5, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: Buschke-Ollendorff syndrome
(Source: NLM General Announcements)
Source: NLM General Announcements - November 5, 2013 Category: Databases & Libraries Source Type: news

NLM Mourns Loss of Former New York Congressman Major Owens
Cong. Major Owens (Source: NLM General Announcements)
Source: NLM General Announcements - October 31, 2013 Category: Databases & Libraries Source Type: news

MedlinePlus Connect Integrates Information from Genetics Home Reference
The National Library of Medicine has released an enhancement to MedlinePlus Connect, NLM's service for patient portals and electronic health record (EHR) systems.  MedlinePlus Connect makes it easy for EHRs to link to targeted information for patients from MedlinePlus, using their existing coding for diagnoses (problem codes), medications, and laboratory test results. (Source: NLM General Announcements)
Source: NLM General Announcements - October 30, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: leptin receptor deficiency
New Topic on Genetics Home Reference (Source: NLM General Announcements)
Source: NLM General Announcements - October 30, 2013 Category: Databases & Libraries Source Type: news

MedlinePlus: Malformación de Chiari
MedlinePlus: Malformación de Chiari (Source: NLM General Announcements)
Source: NLM General Announcements - October 23, 2013 Category: Databases & Libraries Source Type: news

NLM, AAHSL Announce 2013-2014 Leadership Fellows Program Participants
The National Library of Medicine (NLM) and the Association of Academic Health Sciences Libraries (AAHSL) are pleased to announce the selection of fellows and mentors for the 2013-2014 class of their jointly sponsored leadership program. This will be the twelfth LFP class. (Source: NLM General Announcements)
Source: NLM General Announcements - October 22, 2013 Category: Databases & Libraries Source Type: news

MedlinePlus: Chiari Malformation
(Source: NLM General Announcements)
Source: NLM General Announcements - October 22, 2013 Category: Databases & Libraries Source Type: news

NLM Enhances Online Resource “In His Own Words: Martin Cummings and the NLM”
Martin M. Cummings, MD, with printed volumes of the Index Medicus and in the background, the computer tapes that he intended would replace them (1968). (Source: NLM General Announcements)
Source: NLM General Announcements - October 1, 2013 Category: Databases & Libraries Source Type: news

FAQ: DOCLINE -- Reviewing and Updating DOCLINE Routing Tables
New DOCLINE FAQ: "What should I review in my DOCLINE Routing Table?" (Source: NLM General Announcements)
Source: NLM General Announcements - September 26, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: adolescent idiopathic scoliosis
New Topic on Genetics Home Reference (Source: NLM General Announcements)
Source: NLM General Announcements - September 24, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: Griscelli syndrome
New Topic on Genetics Home Reference (Source: NLM General Announcements)
Source: NLM General Announcements - September 24, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: rheumatoid arthritis
New Topic on Genetics Home Reference (Source: NLM General Announcements)
Source: NLM General Announcements - September 24, 2013 Category: Databases & Libraries Source Type: news

Papers of Lawrence Kolb Sr., Addiction Research Pioneer, Now Digitized
The National Library of Medicine is pleased to announce the completion of its third collaborative digitization project with Gale/Cengage Learning's Archives Unbound service. (Source: NLM General Announcements)
Source: NLM General Announcements - September 24, 2013 Category: Databases & Libraries Source Type: news

NLM Lends Collections to Grolier Club Exhibition “Extraordinary Women in Science and Medicine: Four Centuries of Achievement ”
The National Library of Medicine (NLM) is pleased to be a part of a new exhibition on view until November 23, 2013 at The Grolier Club in New York City. (Source: NLM General Announcements)
Source: NLM General Announcements - September 18, 2013 Category: Databases & Libraries Source Type: news

Genetics Home Reference: TK2-related mitochondrial DNA depletion syndrome, myopathic form
New Topic on Genetics Home Reference (Source: NLM General Announcements)
Source: NLM General Announcements - September 17, 2013 Category: Databases & Libraries Source Type: news