Results 241 to 250 of about 238,541 (307)

Trametinib restores the central conducting lymphatic flow in a premature infant with Noonan syndrome. [PDF]

Clin Case Rep
Leenders EKSM, Kleimeier LER, Weeke LC, Coppens CH, Klein WM, Draaisma JMT.   +5 more
europepmc   +1 more source

Cardiac Dysfunction Associated with Lacosamide in a Premature Infant with Hypoxic Ischemic Encephalopathy: A Case Report. [PDF]

AJP Rep
Chatmethakul T, Stanford AH, Rios DR, Bischoff AR, Czech T, McNamara PJ.   +5 more
europepmc   +1 more source

An Interactive Preoperative Virtual Reality Intervention for Breast Cancer Patients Undergoing Oncological Surgery: A Feasibility and Pilot Randomized Clinical Trial

Journal of Surgical Oncology, EarlyView.
ABSTRACT Background and Objectives Preoperative anxiety is common before surgery and is associated with adverse outcomes, yet access to mental health support remains limited. We evaluated the feasibility and acceptability of a novel preoperative virtual reality (VR) prototype designed to reduce anxiety in patients undergoing cancer surgery.
Renée El‐Gabalawy, Gabrielle S. Logan, Pamela Hebbard, Jordana L. Sommer, Kristin Reynolds, Kailey E. Penner, Michael S. D. Smith, Natalie Mota, W Alan C. Mutch, Eisi Mollanji, Jessica L. Maples‐Keller, David Perrin, Rakesh C. Arora   +12 more
wiley   +1 more source

Acquired methemoglobinemia in a third trimester puerpera and her premature infant with sodium nitrite poisoning: A case report. [PDF]

World J Clin Cases
Fei DS, Gao Y, Bao XJ, Tang YJ, Lin YL, Xu JX, Zhang JN, Liu BW, Kang K.   +8 more
europepmc   +1 more source

First Report of Homozygous COL7A1 c.5756delG Mutation Causing Recessive Dystrophic Epidermolysis Bullosa in a Non‐Consanguineous Japanese Family

JEADV Clinical Practice, EarlyView.
ABSTRACT Severe recessive dystrophic epidermolysis bullosa (RDEB) is usually caused by biallelic loss‐of‐function mutations in COL7A1. While the c.5756delG variant has been previously reported in heterozygous form, its clinical impact in homozygosity has not been described.
Nozomi Kohama, Sayaka Yamaguchi, Teruki Yanagi, Yumi Akamine, Kimiko Nonaka, Daisuke Utsumi, Kenzo Takahashi   +6 more
wiley   +1 more source

Draft Genome Sequence of Candida saopaulonensis from a Very Premature Infant with Sepsis. [PDF]

Mycopathologia
Ning YT, Dai RC, Luo ZY, Xiao M, Xu Y, Yan Q, Zhang L.   +6 more
europepmc   +1 more source

Evaluating Neurodevelopmental Sequelae of Propranolol Use in Infantile Hemangioma: A Large‐Scale Population‐Based Study

JEADV Clinical Practice, EarlyView.
ABSTRACT Background Propranolol is widely adopted as the first‐line treatment for problematic infantile hemangioma (IH). Despite its efficacy and widespread use, concerns persist about potential long‐term neurodevelopmental risks, given propranolol′s ability to cross the blood‐brain barrier during early development. Objectives To evaluate the long‐term
Khalaf Kridin, Samer Kridin, Wisal Sawaed, Ralf J. Ludwig   +3 more
wiley   +1 more source

El recién nacido pretérmino con infección de inicio precoz

Revista de Ciencias Médicas de Pinar del Río
Natacha Alessandrini Garaboa, Yanett Sarmiento Portal, Yiliani Marquez Concepción, María Elena Portal Miranda, Omar León Vara Cuesta   +4 more
doaj  

Early Acitretin Therapy in a Patient With Harlequin Ichthyosis

JEADV Clinical Practice, EarlyView.
ABSTRACT Harlequin ichthyosis (HI) is a rare, severe congenital disorder of keratinization caused by pathogenic variants in the ABCA12 gene resulting in thick, hyperkeratotic plates, deep fissures, and characteristic facial and limb abnormalities.
Orasa Sukmark, Parith Wongkittichote, Sanchawan Wittayakornrerk   +2 more
wiley   +1 more source

Comparing sucrose solution with distilled water for pain management in premature infant venipuncture: randomized clinical trial. [PDF]

Ann Med Surg (Lond)
Habibzadeh H, Salamat Bakhsh M, Hosseini M, Khalkhali HR.   +3 more
europepmc   +1 more source