Results 291 to 300 of about 1,925,273 (360)

Growth Hormone Treatment in Patients With KBG Syndrome: Novel Insights, Challenges and Recommendations From Six New Patients and Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT KBG syndrome is one of the most frequent neurodevelopmental disorders and is caused by ANKRD11 variants. Postnatal short stature is observed in ~50% of patients. Recombinant human growth hormone (rhGH) has become a valuable treatment for patients with growth hormone deficiency (GHD) along with Prader–Willi and Turner syndrome. Limited evidence
Sietse M. Aukema   +19 more
wiley   +1 more source

Silent Danger: Risk Factors and Outcomes of Fortuitously Discovered Uterine Rupture - A 41-Case Cohort Study. [PDF]

open access: yesF1000Res
Karmous N   +6 more
europepmc   +1 more source

Unraveling the Genomic Architecture of Supernumerary (Iso‐)Dicentric Chromosomes in Dup15q Syndrome: Insight From a Systematic Literature‐Based Study

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Chromosomal aberrations, particularly copy‐number variations (CNVs), are prevalent in neurodevelopmental disorders (NDD) and significantly contribute to their pathogenesis. Copy‐number gains (CN gains) in 15q11‐q13, primarily consisting of a pseudo (iso‐)dicentric chromosome 15 [(i)dic(15)] or an interstitial duplication, are among the most ...
Sebastian Burkart   +5 more
wiley   +1 more source

Pregnancy and Dry Eye Syndrome: A Review for Clinical Practice. [PDF]

open access: yesInt J Mol Sci
Jaruchowska M   +2 more
europepmc   +1 more source

Management of Odontogenic Infections in Pregnant Patients: Case-Based Approach and Literature Review. [PDF]

open access: yesPathogens
Hramyka A   +9 more
europepmc   +1 more source

Postpartum QT Prolongation in a Long QT Syndrome Type 1 Patient. [PDF]

open access: yesAnn Noninvasive Electrocardiol
Wiedenmann LC, Ehrlich JR, Goldenberg I.
europepmc   +1 more source

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