Results 231 to 240 of about 73,873 (328)

Evaluating the Effectiveness of Nasoalveolar Molding in the Management of Children with Unilateral Cleft Lip and Palate: A Cohort Study. [PDF]

open access: yesDent J (Basel)
España-Guerrero A   +7 more
europepmc   +1 more source

Diagnosis of femoral hypoplasia-unusual facies syndrome in the fetus. [PDF]

open access: yes, 2007
D'ARMIENTO, MARIA   +6 more
core   +1 more source

Linking Health Financing to Oral Health Coverage and Disease Burden in SEARO Countries: A Cross‐Sectional Analysis of Country Level Data

open access: yesThe International Journal of Health Planning and Management, Volume 41, Issue 1, Page 47-58, January 2026.
ABSTRACT Introduction The Southeast Asian region of World Health Organization (SEARO) comprising 11 countries, that is Bangladesh, Bhutan, Democratic People's Republic of Korea, India, Indonesia, Maldives, Myanmar, Nepal, Sri Lanka, Thailand, and Timor‐Leste is home to a quarter of the world's population where severe oral health disparities persist ...
Shashidhar Acharya   +3 more
wiley   +1 more source

Dr. Charles Pinto

open access: yesIndian Journal of Plastic Surgery, 2009
H. S. Adenwalla
doaj   +1 more source

Effects of Food Preferences and Supplement Intake During Pregnancy on the Cleft Lip and Palate Incidence: The Japan Environment and Children's Study. [PDF]

open access: yesNutrients
Fujiwara K   +9 more
europepmc   +1 more source

Basal Cell Nevus Syndrome Treated With Laser Therapy: Novel Approach for Young Adults

open access: yes
International Journal of Dermatology, Volume 65, Issue 2, Page 362-364, February 2026.
Giulia Briatico   +4 more
wiley   +1 more source

Identification and Functional Characterization of a Novel SEMA3A Exon Deletion Variant in Kallmann Syndrome

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.
The study identified a novel SEMA3A exons 6–9 deletion variant in Kallmann syndrome that impairs GnRH neuronal migration and alters cell migration, gonad development, and synaptic pathways. The study expands mutation spectrum and offers mechanistic insights for clinical diagnosis of Kallmann syndrome.
Shaolian Zang   +4 more
wiley   +1 more source

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