Results 91 to 100 of about 307,837 (351)
Nigerian Journal of Surgery, 2017 Background: Procedure-related and patient-related factors influence the prognosis of dental implants to a major extent. Hence, we aimed to evaluate and analyze various systemic factors in patients receiving dental implants.
Sanjay Byakodi +6 more
doaj +1 more source
Homo heidelbergensis: The Tool to Our Success [PDF]
, 2016 Homo heidelbergensis, a physiological variant of the species Homo sapien, is an extinct species that existed in both Europe and parts of Asia from 700,000 years ago to roughly 300,000 years ago (carbon dating). This “subspecies” of Homo sapiens, as it is
Burkard, Alexander
core +1 more source
Growth Standards for Children With Smith–Magenis Syndrome (SMS)
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Smith–Magenis syndrome (SMS, OMIM 182290) is a complex syndromic diagnosis marked by neurobehavioral differences and distinct facial dysmorphisms, caused by haploinsufficiency of the retinoic acid‐1 (RAI1) gene either by a pathogenic sequence variant or deletion at chromosome 17p11.2 involving a portion or all of this gene.
Julie Hoover‐Fong +10 more
wiley +1 more source
Fully guided implant surgery using Magnetic Resonance Imaging – An in vitro study on accuracy in human mandibles [PDF]
, 2020 Tabea Flügge +5 more
openalex +1 more source
Sex determination of human mandible using metrical parameters.
Journal of clinical and diagnostic research : JCDR, 2013 INTRODUCTION Determination of sex from an unknown human bone is an important role in forensic and anthropology field. The mandible is the largest and hardest facial bone, that commonly resist post mortem damage and forms an important source of ...
V. G, Mangala Gowri S R, A. J
semanticscholar +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 +14 more
wiley +1 more source
Uppermost Pleistocene shrews (Mammalia, Soricidae) from Vaskapu Cave (N-Hungary) [PDF]
, 1999 Three shrew species (Sorex araneus LINNAEUS1758, Sorex minutus LlNNAEUS1766 and Sorex alpinus SHINZ1837) were found in the fossiliferous sediments of Vaskapu Cave, near Felsötárkány.
Mészáros, L. Gy.
core
New Species and Additional Records of Protura from Michigan [PDF]
, 2017 Three new species, Eosentomon antrimense, E. pinusbanksianum, and Berberentulus mcqueeni, and one new record, E. australicum Womersley are added to the known Protura fauna of Michigan. Further records of E.
B, Ernest C, Bernard
core +2 more sources
The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley +1 more source
International Forum of Allergy &Rhinology, EarlyView.ABSTRACT Objective In the last two decades, transnasal endoscopic surgery (TES) has become pivotal in the management of sinonasal tumors. This approach involves a multiblock tumor resection, adding complexity to the interpretation of surgical margins after pathological examination.
Piergiorgio Gaudioso +14 more
wiley +1 more source