Results 211 to 220 of about 32,017 (312)

Lymphatic Abnormalities in Noonan Syndrome Extend Beyond Clinically Apparent Disease

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Lymphatic disease represents a well‐described manifestation of Noonan syndrome (NS), yet the full phenotypic spectrum remains incompletely characterized, especially in asymptomatic individuals. We conducted a cross‐sectional study including 10 individuals with NS (four with peripheral lymphedema and six without) and 10 age‐ and sex‐matched ...
Inger Norlyk Sheyanth, Benjamin Kelly, Sheyanth Mohanakumar, Steffen Ringgaard, Yoav Dori, Irene Kibæk Nielsen, Uffe Birk Jensen, Vibeke Elisabeth Hjortdal   +7 more
wiley   +1 more source

Geographic differentiation of ectoparasitic flatworms in the pelagic zone of Lake Tanganyika, Africa. [PDF]

Front Zool
Kmentová N, Thys KJM, Hahn C, Vorel J, Bachmann L, Koblmüller S, Van Steenberge M, Chocha Manda A, Makasa L, Mulimbwa N'Sibula T, Masilya Mulungula P, Vanhove MPM.   +11 more
europepmc   +1 more source

De Novo Complex Genomic Rearrangement Spanning 2q31.1 in a Proband With Congenital Malformations: Genotype–Phenotype Correlation and Development of a CGR Detection Pipeline

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The 2q31 region is commonly associated with pathogenic alleles of the HOXD cluster leading to various clinical phenotypes related to skeletal development. We present a proband with tetralogy of Fallot and multiple congenital anomalies. Genomic variant screening including an in‐house CGR detection pipeline pairing genome sequencing (GS ...
Katherine Helle, Jesse D. Bengtsson, Mira Gandhi, Christopher M. Grochowski, Ming Yin Lun, Neha Sudhir, Shalini N. Jhangiani, Fritz J. Sedlazeck, Seema R. Lalani, Neil A. Hanchard, Claudia M. B. Carvalho   +10 more
wiley   +1 more source

Unlocking the potential of other effective area-based conservation measures (OECMs) for achieving conservation targets: A global scoping review. [PDF]

Ambio
Petza D, Amorim E, Lamine EB, Colloca F, Dominguez Crisóstomo E, Fabbrizzi E, Fraschetti S, Galparsoro I, Giakoumi S, Kruse M, Stelzenmüller V, Katsanevakis S.   +11 more
europepmc   +1 more source

Fisheries Policy, the World Fisheries Crisis and Policy Reforms of the U.S.A. and the Falkland Islands

Fisheries Policy, the World Fisheries Crisis and Policy Reforms of the U.S.A. and the Falkland Islands
The fishing industries of the world are currently in a crisis brought about mainly by overfishing : the capture of too many fish such that the population cannot recover and so collapses dramatically. This paper considers how overfishing occurs, its wider effects and what might be done to control it. Brief reference is made to the history of attempts to
openaire  

Vascular Abnormalities in Hypermobile Ehlers–Danlos Syndrome: A Retrospective Cohort Study

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Hypermobile Ehlers–Danlos syndrome (hEDS), while generally free from severe vascular complications, may occasionally present with cardiac and vascular abnormalities that warrant specific investigation. While studies have been conducted on the prevalence of cardiac involvement, none have focused on vascular aspects. This retrospective study was
Thomas Gehin, Malika Foy, Robert Carlier, Valentin Renault, Karelle Benistan   +4 more
wiley   +1 more source

Systemic approaches for the protection of our oceans and marine environments. [PDF]

NPJ Clim Action
Koundouri P, Akinsete E, Capon T, Colwell RR, El-Beltagy AS, Elouafi I, Falk J, Garabato AN, Kennel CF, Landis C, Leinen M, Mashayek A, Murray CA, Serageldin I, Takeuchi K, Taniguchi M, Toli E.   +16 more
europepmc   +1 more source

Clinical Outcomes and Patient Experiences With Celiprolol Therapy in Vascular Ehlers–Danlos Syndrome: The First Non‐European Cohort

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Vascular Ehlers–Danlos syndrome (vEDS) is a hereditary connective tissue disorder caused by heterozygous pathogenic variants in COL3A1. European studies have shown that celiprolol may reduce the risk of life‐threatening vascular events, but outcomes in non‐European populations and the therapy's psychological impact remain unclear. We conducted
Megumi Furuhata‐Yoshimura, Tomomi Yamaguchi, Tomoki Kosho   +2 more
wiley   +1 more source

The Efficacy of Fisheries Management: A Length-Based Stock Assessment of Eight Fish Species in Xingkai Lake, China. [PDF]

Animals (Basel)
Zhao C, Gao Z, Wang X, Wang W, Wang H, Wang L, Huo T.   +6 more
europepmc   +1 more source

Expanding the Utility of Exome Sequencing in Preventive and Population Genetics

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Carrier screening is a long‐standing genetic testing process offered to at‐risk couples, with or without a family history, who might have pregnancies affected by an autosomal recessive (AR) or X‐linked (XL) disorder. A total of 276 unrelated individuals, initially referred for rare disorder screening by clinicians, were enrolled in this study ...
Charilaos Kostoulas, Athanasia Sesse, Ioanna Bouba, Robert Najdecki, Spyridon Konitsiotis, Sofia Markoula, Ioannis Georgiou   +6 more
wiley   +1 more source