Results 71 to 80 of about 284,684 (201)

Genetic regulation of pituitary gland development in human and mouse [PDF]

open access: yes, 2009
Normal hypothalamopituitary development is closely related to that of the forebrain and is dependent upon a complex genetic cascade of transcription factors and signaling molecules that may be either intrinsic or extrinsic to the developing Rathke’s ...
Aarskog   +321 more
core   +2 more sources

Anatomia cirúrgica do acesso nasal transesfenoidal para tumores da hipófise Surgical anatomy of the nasal transphenoidal approach for pituitary tumors

open access: yesArquivos de Neuro-Psiquiatria, 1997
Foram analisadas diferentes medidas relacionadas ao acesso nasal transesfenoidal em 18 hemicabeças de cadáveres com o objetivo de estudar os limites e vantagens dessa via.
Murilo S. Meneses   +6 more
doaj   +1 more source

Schwannoma de septo nasal: avaliação de massa nasal unilateral Schwannoma of the nasal septum: evaluation of unilateral nasal mass

open access: yesBrazilian Journal of Otorhinolaryngology, 2013
Henrique Furlan Pauna   +4 more
doaj   +1 more source

Aspectos métricos y morfoscópicos de la región nasal en vascos. [PDF]

open access: yes, 1987
Se han estudiado algunos caracteres métricos y descriptivos de la región nasal, en una población vasca femenina y masculina, de Vizcaya y Guipúzcoa. En los dos sexos la nariz es alta, muy   leptorrina, con el perfil recto o convexo - ondulado.
Esther Rebato
core  

Routine 36‐week scan: diagnosis of fetal abnormalities

open access: yesUltrasound in Obstetrics &Gynecology, Volume 65, Issue 4, Page 427-435, April 2025.
ABSTRACT Objectives To investigate further the incidence and types of fetal abnormality identified at a routine 36‐week ultrasound examination, which had not been diagnosed in previous scans at 20 weeks and 12 weeks' gestation, and to report the fetal abnormalities that are diagnosed only postnatally.
A. Syngelaki   +5 more
wiley   +1 more source

Estudio de tumores de la cavidad nasal y senos paranasales del perro mediante tomografía computarizada [PDF]

open access: yes, 2007
En 8 perros se estudiaron imágenes de tomografía computarizada (TC), analizando la extensión de tumores de cavidad nasal y/o senos paranasales. La técnica resultó especialmente útil en animales con descarga nasal crónica, protrusión del globo ocular ...
Blanco Navas, Beatriz   +3 more
core  

Adaptation and validation of the Dutch version of the nasal obstruction symptom evaluation (NOSE) scale [PDF]

open access: yes, 2017
The nasal obstruction symptom evaluation (NOSE) scale is a validated disease-specific, self-completed questionnaire for the assessment of quality of life related to nasal obstruction.
Datema, F.R. (Frank)   +2 more
core   +1 more source

Short‐ and Long‐Term Outcomes of Prenatally Identified Congenital Aqueductal Stenosis by Fetal MRI

open access: yesPrenatal Diagnosis, Volume 44, Issue 13, Page 1574-1584, December 2024.
ABSTRACT Objective Providing accurate prenatal prognostication for expectant parents is challenging due to limited literature on factors impacting outcomes in children with congenital aqueductal stenosis (CAS). This study stratified CAS patients into isolated or complex categories (presence of additional intra‐ or extra‐cranial anomalies or genetic ...
Noah J. Smith   +5 more
wiley   +1 more source

Society for endocrinology guideline for understanding, diagnosing and treating female hypogonadism

open access: yesClinical Endocrinology, Volume 101, Issue 5, Page 409-442, November 2024.
Abstract Female hypogonadism (FH) is a relatively common endocrine disorder in women of premenopausal age, but there are significant uncertainties and wide variation in its management. Most current guidelines are monospecialty and only address premature ovarian insufficiency (POI); some allude to management in very brief and general terms, and most ...
Channa N. Jayasena   +13 more
wiley   +1 more source

Expanding the spectrum of phenotypes for MPDZ: Report of four unrelated families and review of the literature

open access: yesClinical Genetics, Volume 106, Issue 4, Page 413-426, October 2024.
We review MPDZ genetic variants in 18 patients and additional cases from four new families, confirming a range of conditions including hydrocephaly and hearing loss, while introducing a new association with spasticity. A murine model confirms severe hearing impairment, broadening the spectrum of MPDZ‐related diseases. Abstract MPDZ, a gene with diverse
Aboulfazl Rad   +10 more
wiley   +1 more source

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