retrognathia/edema

Veza se sprema u međuspremnik

ČlanciKliničkim ispitivanjimaPatenti

Odaberite vrstu sortiranja

7 rezultati

Modification of the sagittal ramus-split osteotomy for retrognathia.

Samo registrirani korisnici mogu prevoditi članke

Prijavite se / prijavite se

A modification of the sagittal ramus split osteotomy for mandibular advancement has been described. It prevents rotation of the distal fragment, simplifies fixation, and reduces lateral pharyngeal edema.

Minor anomalies in stillborn and second trimester miscarried fetuses.

Samo registrirani korisnici mogu prevoditi članke

Prijavite se / prijavite se

In 1964, the landmark paper of Marden, Smith, and McDonald established that multiple minor anomalies in newborn infants are associated with an increased risk for major malformations. There were until now no comparable studies in stillbirths. The Wisconsin Stillbirth Service Program (WiSSP) has data

The fetal phenotype of the 18p-syndrome. Report of a male fetus at twenty-one weeks.

Samo registrirani korisnici mogu prevoditi članke

Prijavite se / prijavite se

Morphological and cytogenetic findings in a male fetus at 21 weeks gestation after prenatally detected monosomy 18p are reported. The fetus displayed dysmorphic features resembling the 18p-syndrome, such as decreased head circumference, slightly receding forehead, hypertelorism, epicanthus,

Repeated anesthetic management for a patient with Klippel-Feil syndrome.

Samo registrirani korisnici mogu prevoditi članke

Prijavite se / prijavite se

Klippel-Feil syndrome (KFS) is a rare disease characterized by a classic triad comprising a short neck, a low posterior hairline, and restricted motion of the neck due to fused cervical vertebrae. We report repeated anesthetic management for orthognathic surgeries for a KFS patient with

Neu-Laxova syndrome: prenatal ultrasonographic diagnosis, clinical and pathological studies, and new manifestations.

Samo registrirani korisnici mogu prevoditi članke

Prijavite se / prijavite se

A diagnosis of the Neu-Laxova syndrome (NLS) was made by ultrasonography at 32 wks of gestation. Ultrasonographic examination showed intrauterine growth retardation (IUGR), Dandy-Walker anomaly, choroid plexus cysts, receding forehead and microcephaly, bilateral cataract without prominent eyes,

MR Imaging of the Temporomandibular Joint in Juvenile Idiopathic Arthritis: Technique and Findings.

Samo registrirani korisnici mogu prevoditi članke

Prijavite se / prijavite se

The term juvenile idiopathic arthritis (JIA) encompasses a group of arthritides of unknown cause that begin before 16 years of age and last for at least 6 weeks. Temporomandibular joint (TMJ) involvement has been described in up to 87% of children with JIA and has been associated with all JIA

Characteristic dysmorphic features in congenital disorders of glycosylation type IIb.

Samo registrirani korisnici mogu prevoditi članke

Prijavite se / prijavite se

Over 100 types of congenital disorders of glycosylation (CDG) have been reported and the number is rapidly increasing. However, each type is very rare and is problematic to diagnose. Mannosyl-oligosaccharide glucosidase (MOGS)-CDG (CDG type IIb) is an extremely rare CDG that has only been reported

Pridružite se našoj
facebook stranici

Herbal & Natural Medicine

Najkompletnija baza ljekovitog bilja potpomognuta naukom

Radi na 55 jezika
Biljni lijekovi potpomognuti naukom
Prepoznavanje biljaka po slici
Interaktivna GPS karta - označite bilje na lokaciji (uskoro)
Pročitajte naučne publikacije povezane sa vašom pretragom
Pretražite ljekovito bilje po učincima
Organizirajte svoja interesovanja i budite u toku sa istraživanjem vijesti, kliničkim ispitivanjima i patentima

Upišite simptom ili bolest i pročitajte o biljkama koje bi mogle pomoći, unesite travu i pogledajte bolesti i simptome protiv kojih se koristi.
* Sve informacije temelje se na objavljenim naučnim istraživanjima