Results 191 to 200 of about 1,427,784 (294)

The impact of day care attendance on antibiotic use among children aged 0-12 years: A population-based register study. [PDF]

PLoS One
Räsänen T, Saarikallio-Torp M, Rättö H, Kari H.   +3 more
europepmc   +1 more source

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää, Chad R. Haldeman‐Englert, Marja Hietala, Melisa S. Tanverdi, Patrick P. Koty, Diana Brightman, Eniolami Dosunmu, Shailja Tibrewal, Savleen Kaur, Anupriya Kaur, Raj Kumar Verma, Alejandra G. de Alba Campomanes, Virginia Utz, Anne M. Slavotinek, Cynthia Curry   +14 more
wiley   +1 more source

Five-year follow-up of patients with low-risk papillary thyroid cancer treated without postoperative radioiodine: prospective study by the Finnish Thyroid Cancer Group. [PDF]

Acta Oncol
Halonen P, Salo M, Ahtiainen V, Matikainen N, Aula H, Ruohola J, Moilanen L, Koivikko M, Metso S, Peurala E, Mäenpää H, Finnish Thyroid Cancer Group.   +11 more
europepmc   +1 more source

Online-Only Abstracts: Population-based burden of bloodstream infections in Finland [PDF]

, 2012

openalex   +1 more source

Genotypes and Phenotypes of Patients With TSPEAR‐Related Disorder: Evidence of a Predominant Dental Phenotype

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani, Lucia Tiberi, Annarita Giliberti, Elia Dirupo, Laila Zaroili, Francesco Brancati, Michela Brena, Stefano Caraffi, Chiara De Luca, Livia Garavelli, Anna Virginia Gulino, Milena Mariani, Marzia Pollazzon, Angelo Selicorni, Samuela Landini, Ilaria Sani, Rosangela Artuso, Angela Peron   +17 more
wiley   +1 more source

Unexpected species richness of the lichen genus <i>Protoblastenia</i> (Lecanorales, Psoraceae) in Finland. [PDF]

MycoKeys
Pykälä J, Myllys L.
europepmc   +1 more source

“Ghosts in the background” and “The price of the war”. Representations of the Lapland War in Finnish museums

, 2017
Suzie Thomas, Eerika Koskinen-Koivisto
openalex   +2 more sources

Molecular Profiling of Genes Associated With Methylphenidate Pathway Therapy and Discovery of New Variants in Amazonian Amerindian Populations

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT In Attention Deficit Hyperactivity Disorder (ADHD), methylphenidate is one of the most widely used drugs, in which patient response significantly impacts prognosis. This study aimed to characterize the molecular profile of 10 genes associated with methylphenidate therapy.
Aline Pasquini Santos, Tatiane Carinta de Souza, Kaio Evandro Cardoso Aguiar, Ana Caroline Alves da Costa, Natasha Monte, Juliana Carla Gomes Rodrigues, Giovanna Gilioli da Costa Nunes, Rita de Cássia Calderaro Coelho, Ândrea Ribeiro‐dos‐Santos, André Maurício Ribeiro dos Santos, Sandro José de Souza, Sidney Emanuel Batista dos Santos, Rommel Mario Rodriguez Burbano, Marianne Rodrigues Fernandes, Ney Pereira Carneiro dos Santos   +14 more
wiley   +1 more source

Are We Doing Enough? Drug-Related Deaths as a Pressing Social Issue. [PDF]

Nordisk Alkohol Nark
Karjalainen K, Pekka H, Sanna R.
europepmc   +1 more source

Physical Activity and Learning Environment Qualities in Finnish Day Care

, 2012
Anna-Liisa Kyhälä, Jyrki Reunamo, Heikki Ruismäki   +2 more
openalex   +1 more source