Results 201 to 210 of about 678,857 (336)

Introducing last planner : Finnish experiences [PDF]

The Last Planner method1 represents a radically different manner of controlling production in construction. Even if its benefits are widely observed, it is also a common observation that the introduction of the Last Planner method to a site, into a ...
Koskela, Lauri, Koskenvesa, Anssi
core  

Dentofacial Malocclusion in Neurofibromatosis 1 in Finland

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Neurofibromatosis 1 (NF1) is an inherited disease that can be accompanied by oral health problems such as caries, periodontitis, and tumors affecting the oral cavity. Also, different maxillary and mandibular malformations are associated with NF1.
Vivian Reinhold, Mikko Valtanen, Kari Auranen, Stina Syrjänen, Sirkku Peltonen, Juha Peltonen, Roope A. Kallionpää   +6 more
wiley   +1 more source

Loss of CFHR5 function reduces the risk for age-related macular degeneration. [PDF]

Nat Commun
Reeve MP, Loomis S, Nissilä E, Soare TW, Rausch T, Zheng Z, Della Briotta Parolo P, Ben-Isvy D, Aho E, Cesetti E, Okunuki Y, McLaughlin H, Mäkelä J, FinnGen, Kurki M, Talkowski ME, Korbel JO, Connor K, Meri S, Daly MJ, Runz H.   +20 more
europepmc   +1 more source

Survey of forest technology research in Finland [PDF]

, 1959
Theodor Wegelius
openalex   +1 more source

What is Left to Residual Claimants? The Empirics of Income Reported by Entrepreneurs and Workers [PDF]

Using Finnish panel data, we study how entrepreneurs differ from workers in education and income dynamics. We find that workers have higher median income in all educational groups.
Juha Tuomala, Panu Poutvaara
core  

Genome‐Wide Insights and Polygenic Risk Scores in Common Epilepsies: A Narrative Review

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT The research of single gene‐related disorders or pathogenic copy‐number variations (CNVs) has given a significant impetus to the shift from a diagnostic work‐up focused on epileptic syndromes to genomic approaches in individuals with severe pediatric‐onset epilepsies and in developmental and epileptic encephalopathies.
Mario Mastrangelo, Simona Petrucci, Giuliana Lentini, Marco Fabiani, Maria Piane, Francesco Pisani   +5 more
wiley   +1 more source

Medical Students' Perceptions of the Best Clinical Teaching. [PDF]

Clin Teach
Hannula V, Lehtovirta L, Liu H, Sumanen M.   +3 more
europepmc   +1 more source

Education and invention. [PDF]

Modern growth theory puts invention on the center stage. Inventions are created by individuals, raising the question: can we increase number of inventors? To answer this question, we study the causal effect of M.Sc.
Toivanen, Otto, Väänänen, Lotta
core  

Parental Decision‐Making Following a Prenatal Diagnosis of Turner Syndrome: A Systematic Review

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT This systematic review investigates factors influencing parental decision‐making following a prenatal diagnosis (PND) of Turner syndrome (TS), aiming to enhance the foundation for tailored and supportive genetic counseling. A comprehensive literature search was conducted in the medical databases PubMed, Embase, and CINAHL.
Inger Lily Hjuler Dorf, Stina Lou, Anne Skakkebæk   +2 more
wiley   +1 more source

Cancer risk after preeclampsia: a cohort study in two Nordic populations. [PDF]

BJC Rep
Vesterlund G, Mao X, Gissler M, Abedi-Valugerdi M, Skoog T, Heinonen S, Sparen P, Pettersson K, Kere J, Czene K, Wedenoja S.   +10 more
europepmc   +1 more source