Clinical Management of Congenital Hypogonadotropic Hypogonadism von Young, Jacques, Xu, Cheng, Papadakis, Georgios E, Acierno, James S, Maione, Luigi, Hietamäki, Johanna, Raivio, Taneli, Pitteloud, Nelly

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The GPR54 Gene as a Regulator of Puberty von Seminara, Stephanie B, Messager, Sophie, Chatzidaki, Emmanouella E, Thresher, Rosemary R, Acierno, James S, Shagoury, Jenna K, Bo-Abbas, Yousef, Kuohung, Wendy, Schwinof, Kristine M, Hendrick, Alan G, Zahn, Dirk, Dixon, John, Kaiser, Ursula B, Slaugenhaupt, Susan A, Gusella, James F, O'Rahilly, Stephen, Carlton, Mark B.L, Crowley, William F, Aparicio, Samuel A.J.R, Colledge, William H

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Thermal conductivity and dielectric properties of polypropylene‐based hybrid compounds containing multiwalled carbon nanotubes von Russo, P., Patti, A., Petrarca, C., Acierno, S.

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Mutations in Fibroblast Growth Factor Receptor 1 Cause Both Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism von Pitteloud, Nelly, Acierno, James S., Meysing, Astrid, Eliseenkova, Anna V., Ma, Jinghong, Ibrahimi, Omar A., Metzger, Daniel L., Hayes, Frances J., Dwyer, Andrew A., Hughes, Virginia A., Yialamas, Maria, Hall, Janet E., Grant, Ellen, Mohammadi, Moosa, Crowley, William F.

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Alginate–hyaluronan composite hydrogels accelerate wound healing process von Catanzano, O., D’Esposito, V., Acierno, S., Ambrosio, M.R., De Caro, C., Avagliano, C., Russo, P., Russo, R., Miro, A., Ungaro, F., Calignano, A., Formisano, P., Quaglia, F.

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Biotin-Responsive Basal Ganglia Disease Maps to 2q36.3 and Is Due to Mutations in SLC19A3 von Zeng, Wen-Qi, Al-Yamani, Eiman, Acierno, James S., Slaugenhaupt, Susan, Gillis, Tammy, MacDonald, Marcy E., Ozand, Pinar T., Gusella, James F.

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Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome von Barraud, Sara, Delemer, Brigitte, Poirsier-Violle, Céline, Bouligand, Jérôme, Mérol, Jean-Claude, Grange, Florent, Higel-Chaufour, Brigitte, Decoudier, Bénédicte, Zalzali, Mohamad, Dwyer, Andrew A., Acierno, James S, Pitteloud, Nelly , Millar, Robert P., Young, Jacques

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Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel von MEI SUN, GOLDIN, Ehud, COLMAN, Matthew, SCHIFFMANN, Raphael, SLAUGENHAUPT, Susan A, STAHL, Stefanie, FALARDEAU, John L, KENNEDY, John C, ACIERNO, James S, BOVE, Catherine, KANESKI, Christine R, NAGLE, James, BROMLEY, Matthew C

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Concomitant SARS‐CoV‐2 infection and crusted scabies in a 4‐month infant von Giannattasio, A., Rosa, M., Esposito, S., Di Mita, O., Angrisani, F., Acierno, S., D’Anna, C., Barbato, F., Tipo, V., Ametrano, O.

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Nanoscale mechanical characterization of polymers by atomic force microscopy (AFM) nanoindentations: viscoelastic characterization of a model material von Tranchida, D, Kiflie, Z, Acierno, S, Piccarolo, S

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Reversible Kallmann Syndrome, Delayed Puberty, and Isolated Anosmia Occurring in a Single Family with a Mutation in the Fibroblast Growth Factor Receptor 1 Gene von Pitteloud, Nelly, Acierno, James S., Meysing, Astrid U., Dwyer, Andrew A., Hayes, Frances J., Crowley, William F.

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Familial schwannomatosis: Exclusion of the NF2 locus as the germline event von MACCOLLIN, M, WILLETT, C, HEINRICH, B, JACOBY, L. B, ACIERNO, J. S, PERRY, A, LOUIS, D. N

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Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH) von Miura, Kiyonori, Acierno, James S., Seminara, Stephanie B.

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Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes von Pitteloud, Nelly, Meysing, Astrid, Quinton, Richard, Acierno, James S., Dwyer, Andrew A., Plummer, Lacey, Fliers, Eric, Boepple, Paul, Hayes, Frances, Seminara, Stephanie, Hughes, Viriginia A., Ma, Jinghong, Bouloux, Pierre, Mohammadi, Moosa, Crowley, William F.

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A Finite Element Formulation and Nonlocal Theory for the Static and Free Vibration Analysis of the Sandwich Functionally Graded Nanoplates Resting on Elastic Foundation von Pham, Quoc-Hoa, Phung, Minh-Van, Tran, Thanh-Trung, Tran, Van-Ke, Nguyen-Thoi, Trung

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Testosterone-induced increase in libido in a patient with a loss-of-function mutation in the AR gene von Marino, Laura, Messina, Andrea, S Acierno, James, Phan-Hug, Franziska, J Niederländer, Nicolas, Santoni, Federico, La Rosa, Stefano, Pitteloud, Nelly

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A Locus for Autosomal Dominant Mitral Valve Prolapse on Chromosome 11p15.4 von Freed, Lisa A., Acierno, James S., Dai, Daisy, Leyne, Maire, Marshall, Jane E., Nesta, Francesca, Levine, Robert A., Slaugenhaupt, Susan A.

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Optimization of Tensile and Impact Strength for Injection Moulded Nylon 66/Sic/B4c Composites von Boopathy, G., Vanitha, V., Karthiga, K., Gugulothu, Bhiksha, Pradeep, A., Pydi, Hari Prasadarao, Vijayakumar, S.

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β-Klotho deficiency protects against obesity through a crosstalk between liver, microbiota, and brown adipose tissue von Somm, Emmanuel, Henry, Hugues, Bruce, Stephen J, Aeby, Sébastien, Rosikiewicz, Marta, Sykiotis, Gerasimos P, Asrih, Mohammed, Jornayvaz, François R, Denechaud, Pierre Damien, Albrecht, Urs, Mohammadi, Moosa, Dwyer, Andrew, Acierno, Jr, James S, Schoonjans, Kristina, Fajas, Lluis, Greub, Gilbert, Pitteloud, Nelly

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Utilization of Superparamagnetic Iron Oxide Nanoparticles (SPIONs) Impregnated Activated Carbon for Removal of Hexavalent Chromium von Farhana, Aisha, Jenifer Selvarani, A., Samrot, Antony V., Alsrhani, Abdullah, Raji, P., Sahithya, Chamarthy Sai, Jane Cypriyana, P. J., Senthilkumar, P., Ling, Mok Pooi, Yishak, Simon

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